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May 06, 2025

Raritan, NJ

|

Materials Science & Engineering

|

Contract

|

$58 - $72 (hourly estimate)

{"JobID":414625,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.612,"Longitude":40.5869909090909,"Distance":null},"State":"New Jersey","Zip":"08869","ReferenceID":"NNJ-780765","PostedDate":"\/Date(1746551659000)\/","Description":"One of our large MedTech clients is looking for a Clinical Research Scientist to join their team for a 12+ month project. This individual will support multiple class 3 device trials. They will develop and draft clinical trial protocols, informed consents, investigator brochures, and other study materials with minimal supervision, plan for study budgets and collaborate with Clinical Operations to manage the development of Investigator agreements and site contracts within fair market value (FMV), vendor agreements, payments, and financial disclosures. They will partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables and will be responsible for delivery of assigned clinical programs, through effective partnership with the Clinical Operations and core teams, to enable optimized engagement leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOP). This role will entail developing strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders and drafting study reports with minimal supervision for assigned studies to include any annual reports, study close out reports as well as clinical sections for IDE, PMA, 510(k), and other regulatory submissions.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Research Scientist","City":"Raritan","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Strong experience independently writing protocols -Experience writing informed consents -5+ years of experience within MedTech or Pharma -Experience working cross-functionally with \"core teams\" -Clinical Operations background-3+ years experience as a Clinical Scientist/Clinical PM","Skills":"-Experience with either BOA, PMA, NDA submissions (FDA approval) -Experience with PMCF plans -MedTech experience (class 3) -Global Trial experience -Clinical Study Report writing","Industry":"Materials Science \u0026 Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":72.0000,"SalaryLow":57.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large MedTech clients is looking for a Clinical Research Scientist to join their team for a 12+ month project. This individual will support multiple class 3 device trials. They will... develop and draft clinical trial protocols, informed consents, investigator brochures, and other study materials with minimal supervision, plan for study budgets and collaborate with Clinical Operations to manage the development of Investigator agreements and site contracts within fair market value (FMV), vendor agreements, payments, and financial disclosures. They will partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables and will be responsible for delivery of assigned clinical programs, through effective partnership with the Clinical Operations and core teams, to enable optimized engagement leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOP). This role will entail developing strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders and drafting study reports with minimal supervision for assigned studies to include any annual reports, study close out reports as well as clinical sections for IDE, PMA, 510(k), and other regulatory submissions.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 16, 2024

Philadelphia, PA

|

Nurse

|

Contract,Perm Possible

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$40 - $50 (hourly estimate)

{"JobID":381044,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-75.1438181818182,"Longitude":39.9653636363636,"Distance":null},"State":"Pennsylvania","Zip":"19140","ReferenceID":"HPA-733518","PostedDate":"\/Date(1726496059000)\/","Description":"Our client is looking for a clinical research nurse to join their school of medicine team to assist in all research studies for pulmonary diseases. This person will be working between handling clinical visits for inpatient and outpatient trials and then data entry and administrative work. Majority of the role will be handling EKGs and drawing blood from patient volunteers. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual, and coordinate the timely study activation and submission of protocol amendments. We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Research Nurse","City":"Philadelphia","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- PA RN License or compact license - 3+ years experience as a registered nurse (if no clinical research background) - Registered Nurse in Clinical Research, Pulmonology, or ICU - BLS/ CPR cert","Skills":"Experience with pulmonary clinical trials CCRP (Cert Clin Research Prof) certification","Industry":"Nurse","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our client is looking for a clinical research nurse to join their school of medicine team to assist in all research studies for pulmonary diseases. This person will be working between handling... clinical visits for inpatient and outpatient trials and then data entry and administrative work. Majority of the role will be handling EKGs and drawing blood from patient volunteers. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual, and coordinate the timely study activation and submission of protocol amendments. We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 04, 2024

Orange, CA

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EMR Electronic Medical Records

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Contract-to-perm

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$56 - $70 (hourly estimate)

{"JobID":378532,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-117.849727272727,"Longitude":33.7952727272727,"Distance":null},"State":"California","Zip":"92868","ReferenceID":"HSW-730974","PostedDate":"\/Date(1725452045000)\/","Description":"As a technical leader in clinical applications, applies advanced professional concepts and extensive industry knowledge to lead and / or work on medium to large projects of broad scope and complexity. The incumbent provides support for all computer and information systems activities of the Pathology Department. Monitors activity and maintains LIS performance and integrity to ensure highest standards of patient care and compliance with all applicable regulations. Incumbent may be required to chair user group and validation committees with technical specialists and physicians across the Health System. Collaboration: Work with lab leaders, other analysts, section heads, and SMEs to gather preliminary information for builds. Build and Testing: Perform builds, testing, and keep tabs on lab items. Support: Provide ongoing support for Beaker and third-party systems, including rotational on-call duties towards the end of go-live.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Applications Professional IV - Beaker","City":"Orange","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Experience: 3-5 years of experience as a Clinical Application Professional - Beaker Certifications: Beaker CP certification \u0026 CLS/MedTech in California. Skills: Proficiency in Beaker CP. Education: Bachelor\u0027s degree in health care information technology, computer science, or related area, and or equivalent combination of experience/training.","Skills":"Additional Experience: DI experience, HL7 interface experience, Lifepoint experience, and Beaker AP knowledge. Implementation: Prior direct experience with implementations. Knowledge of LIS maintenance, including new test builds Certifications: Epic Beaker Certification, Current California Clinical Lab Scientist or Cytotechnologist License Billing: Experience with EPIC billing.","Industry":"EMR Electronic Medical Records","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

As a technical leader in clinical applications, applies advanced professional concepts and extensive industry knowledge to lead and / or work on medium to large projects of broad scope and... complexity. The incumbent provides support for all computer and information systems activities of the Pathology Department. Monitors activity and maintains LIS performance and integrity to ensure highest standards of patient care and compliance with all applicable regulations. Incumbent may be required to chair user group and validation committees with technical specialists and physicians across the Health System. Collaboration: Work with lab leaders, other analysts, section heads, and SMEs to gather preliminary information for builds. Build and Testing: Perform builds, testing, and keep tabs on lab items. Support: Provide ongoing support for Beaker and third-party systems, including rotational on-call duties towards the end of go-live.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 06, 2025

Malvern, PA

|

Engineering (Non IT)

|

Contract

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$34 - $42 (hourly estimate)

{"JobID":414573,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.5078181818182,"Longitude":40.0437272727273,"Distance":null},"State":"Pennsylvania","Zip":"19355","ReferenceID":"PHL-780531","PostedDate":"\/Date(1746540858000)\/","Description":"The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -- 10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor.Key Responsibilities:-Conduct analytical biological testing of clinical and commercial drug product/drug substance samples-Perform peer reviews and approvals of laboratory data-Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data-Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management -Perform Instrument Calibration and Preventative Maintenance-Update CRS-owned documents using the Document Management System (DMS) -Order/receive supplies and manage inventory-Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities-Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight-Act as a peer subject matter expert in assessing talent by participating in panel interviews for job-Complete invalid assay and general laboratory investigation records-Complete corrective and preventative actions (CAPA) as assigned-Assist in the execution of internal auditsWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"QC Analyst - Clinical Release and Stability","City":"Malvern","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Minimum one year of relevant GMP QC work experience in Pharmaceutical lab-Bachelor degree in Biology or Chemistry-Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs)-Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA-Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols-Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint)","Skills":"-CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience-Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC-Ability to complete equipment and software qualification protocols-Experience developing and setting long-term objectives -Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility-Knowledge of EU/FDA guidance","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":42.0000,"SalaryLow":33.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for... ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -- 10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor.Key Responsibilities:-Conduct analytical biological testing of clinical and commercial drug product/drug substance samples-Perform peer reviews and approvals of laboratory data-Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data-Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management -Perform Instrument Calibration and Preventative Maintenance-Update CRS-owned documents using the Document Management System (DMS) -Order/receive supplies and manage inventory-Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities-Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight-Act as a peer subject matter expert in assessing talent by participating in panel interviews for job-Complete invalid assay and general laboratory investigation records-Complete corrective and preventative actions (CAPA) as assigned-Assist in the execution of internal auditsWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Aug 28, 2024

New York, NY

|

System Administrator

|

Contract

|

$61 - $76 (hourly estimate)

{"JobID":377358,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.9703636363636,"Longitude":40.7209090909091,"Distance":null},"State":"New York","Zip":"10016","ReferenceID":"HTS-729867","PostedDate":"\/Date(1724832873000)\/","Description":"Insight Global is looking for a Technical Ancillary Systems Analyst to join the Clinical Applications and Integrations organization at a large healthcare client in NYC. The Technical Consultant is responsible for Implementing and supporting an assigned portfolio of Clinical Ancillary Applications within one of our largest healthcare clients in Manhattan. They will be responsible for conducting day-to-day communication, monitoring, and maintaining applications. We are looking for someone who demonstrates a deep understanding of clinical operations, and works with vendors, project teams, and the clients Clinical Representatives/Subject Matter Experts, and end users to tailor the system to fit the organizations needs. They will routinely perform in-depth analysis of workflows, data collection, report details, and other technical issues associated with the use of Clinical Ancillary systems. They will be responsible for developing and documenting the internal procedures that will be used in conjunction with assigned Clinical Ancillary applications. They will design, build, test, install, train and maintain those solutions. Having experience with Sterile Processing, Food Services, Temperature Monitoring (SPM, CBORD, Elpro etc.) is highly preferred but any ancillary system knowledge is acceptable. We need someone with experience working with cross functional teams (Servers, Network Security, Interfaces etc.) and willing to come onsite at least 3-4 days a week or whatever is required for the project at that time. The client locations are primarily in Manhattan but this person could also be needed in Long Island and Brooklyn depending on the project.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Ancillary Systems Analyst","City":"New York","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-7+ years of experience in Application Systems Analysis specifically within ancillary systems -Extensive experience troubleshooting and supporting additional ancillary or clinical applications -Experience managing upgrades, roll outs, deployments, documenting and testing of additional applications -Needs to be a go-getter and great communicator to work with stakeholders","Skills":"","Industry":"System Administrator","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":76.0000,"SalaryLow":60.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a Technical Ancillary Systems Analyst to join the Clinical Applications and Integrations organization at a large healthcare client in NYC. The Technical Consultant is... responsible for Implementing and supporting an assigned portfolio of Clinical Ancillary Applications within one of our largest healthcare clients in Manhattan. They will be responsible for conducting day-to-day communication, monitoring, and maintaining applications. We are looking for someone who demonstrates a deep understanding of clinical operations, and works with vendors, project teams, and the clients Clinical Representatives/Subject Matter Experts, and end users to tailor the system to fit the organizations needs. They will routinely perform in-depth analysis of workflows, data collection, report details, and other technical issues associated with the use of Clinical Ancillary systems. They will be responsible for developing and documenting the internal procedures that will be used in conjunction with assigned Clinical Ancillary applications. They will design, build, test, install, train and maintain those solutions. Having experience with Sterile Processing, Food Services, Temperature Monitoring (SPM, CBORD, Elpro etc.) is highly preferred but any ancillary system knowledge is acceptable. We need someone with experience working with cross functional teams (Servers, Network Security, Interfaces etc.) and willing to come onsite at least 3-4 days a week or whatever is required for the project at that time. The client locations are primarily in Manhattan but this person could also be needed in Long Island and Brooklyn depending on the project.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 24, 2024

Henrico, VA

|

EMR Electronic Medical Records

|

Contract

|

$24 - $30 (hourly estimate)

{"JobID":382517,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-77.4504545454545,"Longitude":37.5513636363636,"Distance":null},"State":"Virginia","Zip":"23294","ReferenceID":"HCH-735956","PostedDate":"\/Date(1727169247000)\/","Description":"Project Titles:1. Digital Transformation of Data Capture in Kidney Transplant Referral Evaluation: A Quality Improvement Project2. Kidney HEALTH: The Implementation of e-phenotype to Create an Electronic Health Record-Based Kidney Disease Registry at VCU HealthProject Overviews:1. Kidney Transplant Referral Evaluation Project: This project aims to enhance the efficiency and precision of kidney transplant evaluations through the digital transformation of data received by Hume Lee transplant center for kidney transplant referrals.2. Kidney HEALTH Grant Project: This 2-year project aims to develop a comprehensive kidney disease (KD) registry to support clinical decision-making, improve patient outcomes, and inform population health management. The methodology involves six key steps detailed in Figure 1 and includes three phases: 1) design, 2) development, and 3) implementation.Figure 1. Process for establishing KD patient registry in VCU Health EHRPhase 1. Design Phase 2. Development Phase 3. ImplementationRole: EPIC AnalystObjectives:1. Transplant Referral Assessment Tool Project:? Facilitate requirements gathering for digital transformation of kidney transplant referrals.? Build and customize EPIC forms and other necessary elements.? Interface with the technical team responsible for developing the application.? Ensure the smooth integration of digital tool within the EPIC system.2. Kidney HEALTH Grant Project:? Support the design, development, and implementation of the KD registry.? Collaborate on the six key steps to establish the registry within the EPIC system.? Assist in developing tools and workflows to support clinical decision-making and population health management.Responsibilities:1. Requirements Gathering:? Collaborate with clinical and technical stakeholders to understand project requirements.? Document detailed specifications for EPIC system modifications and enhancements.2. EPIC System Configuration:? Build and customize EPIC forms and workflows to support the kidney transplant referral and KD registry.? Ensure that all EPIC elements are configured correctly and meet the project requirements.3. Technical Coordination:? Serve as the primary point of contact between the project team and the EPIC technical team.? Coordinate the development, testing, and deployment of the electronic forms and KD registry within the EPIC system.4. Quality Assurance:? Conduct thorough testing of the EPIC configurations and the digital forms.? Identify and resolve any technical issues that arise during the implementation phase.5. Documentation and Training:? Develop comprehensive documentation for all EPIC configurations and workflows.? Provide training to end-users on the new system functionalities and workflows.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Epic Analyst- Healthy Planet","City":"Henrico","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Healthy Planet Epic Cert Analytic mindset and background, building dashboards in epic modules","Skills":"clinical background","Industry":"EMR Electronic Medical Records","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":30.0000,"SalaryLow":24.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Project Titles:1. Digital Transformation of Data Capture in Kidney Transplant Referral Evaluation: A Quality Improvement Project2. Kidney HEALTH: The Implementation of e-phenotype to Create an... Electronic Health Record-Based Kidney Disease Registry at VCU HealthProject Overviews:1. Kidney Transplant Referral Evaluation Project: This project aims to enhance the efficiency and precision of kidney transplant evaluations through the digital transformation of data received by Hume Lee transplant center for kidney transplant referrals.2. Kidney HEALTH Grant Project: This 2-year project aims to develop a comprehensive kidney disease (KD) registry to support clinical decision-making, improve patient outcomes, and inform population health management. The methodology involves six key steps detailed in Figure 1 and includes three phases: 1) design, 2) development, and 3) implementation.Figure 1. Process for establishing KD patient registry in VCU Health EHRPhase 1. Design Phase 2. Development Phase 3. ImplementationRole: EPIC AnalystObjectives:1. Transplant Referral Assessment Tool Project:? Facilitate requirements gathering for digital transformation of kidney transplant referrals.? Build and customize EPIC forms and other necessary elements.? Interface with the technical team responsible for developing the application.? Ensure the smooth integration of digital tool within the EPIC system.2. Kidney HEALTH Grant Project:? Support the design, development, and implementation of the KD registry.? Collaborate on the six key steps to establish the registry within the EPIC system.? Assist in developing tools and workflows to support clinical decision-making and population health management.Responsibilities:1. Requirements Gathering:? Collaborate with clinical and technical stakeholders to understand project requirements.? Document detailed specifications for EPIC system modifications and enhancements.2. EPIC System Configuration:? Build and customize EPIC forms and workflows to support the kidney transplant referral and KD registry.? Ensure that all EPIC elements are configured correctly and meet the project requirements.3. Technical Coordination:? Serve as the primary point of contact between the project team and the EPIC technical team.? Coordinate the development, testing, and deployment of the electronic forms and KD registry within the EPIC system.4. Quality Assurance:? Conduct thorough testing of the EPIC configurations and the digital forms.? Identify and resolve any technical issues that arise during the implementation phase.5. Documentation and Training:? Develop comprehensive documentation for all EPIC configurations and workflows.? Provide training to end-users on the new system functionalities and workflows.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 07, 2025

Fayetteville, AR

|

Technical Writer

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":414724,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-94.1458181818182,"Longitude":36.09,"Distance":null},"State":"Arkansas","Zip":"72703","ReferenceID":"BEN-780886","PostedDate":"\/Date(1746609357000)\/","Description":"We are seeking a highly motivated and detail-oriented Epic Beaker Clinical Pathologist to join our team. The ideal candidate will have a strong understanding of clinical pathology workflows and experience working with Epic Beaker.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Epic CP Consultant","City":"Fayetteville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"***Must be certified in: Beaker CP***must be able to travel on site once a month to Northwest Arkansas (NWA)!!! *Must have completed several Epic implementations from start to finish in a healthcare setting. *Strong understanding of clinical workflows and healthcare operations. *Excellent problem-solving and analytical skills. *Strong communication and interpersonal skills. *Ability to work independently and as part of a team * able to commit to a 40 hour work week","Skills":"Bonus certification: Beaker AP (Anatomic Pathology)Expertise with QuestReference lab networkConversions experienceImplementation of data innovation","Industry":"Technical Writer","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

We are seeking a highly motivated and detail-oriented Epic Beaker Clinical Pathologist to join our team. The ideal candidate will have a strong understanding of clinical pathology workflows and... experience working with Epic Beaker.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 06, 2024

Charlottesville, VA

|

Medical Coder

|

Perm

|

$55k - $87k (estimate)

{"JobID":379082,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-78.4709090909091,"Longitude":38.0543636363636,"Distance":null},"State":"Virginia","Zip":"22911","ReferenceID":"HCH-731082","PostedDate":"\/Date(1725610467000)\/","Description":"Insight global is seeking a remote Professional Coding Educator for a healthcare system in Virginia. The educator will provide consulting services to physicians, residents, allied health professionals and billing staff to support patient care documentation, coding and billing practices according to federal, state and local regulatory compliance standards. Creates and delivers presentations to clinical faculty and billing staff.Develops training programs and delivers training and education sessions for physicians, allied health professionals, residents, and coding and billing staff to support compliance with third party documentation and billing regulatory standards, including but not limited to classroom training, web-based training and one-on-one provider observation and training sessions.Participates on clinical department Billing Quality Councils as a member of the respective councils and acts as the primary resource providing technical and regulatory expertise to the Councils.Presents findings and recommendations from internal and external audits to clinical departments and recommends solutions for implementing appropriate changes.Conducts internal reviews and provides quality review of external billing quality audits. Works with providers and department billing staff to address and resolve documentation deficiencies.Develops and implements Clinical Documentation Improvement Programs in partnership with the clinical departments.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Coding Educator/ Auditor","City":"Charlottesville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Requirements: -5 years of experience with coding and coding education-CCS-P or CPC Certification -Experience creating coding presentations for physicians -Experience with Auditing -Experience with academic medical center coding","Skills":"-Neurosurgery exp","Industry":"Medical Coder","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":87000.0000,"SalaryLow":55000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight global is seeking a remote Professional Coding Educator for a healthcare system in Virginia. The educator will provide consulting services to physicians, residents, allied health... professionals and billing staff to support patient care documentation, coding and billing practices according to federal, state and local regulatory compliance standards. Creates and delivers presentations to clinical faculty and billing staff.Develops training programs and delivers training and education sessions for physicians, allied health professionals, residents, and coding and billing staff to support compliance with third party documentation and billing regulatory standards, including but not limited to classroom training, web-based training and one-on-one provider observation and training sessions.Participates on clinical department Billing Quality Councils as a member of the respective councils and acts as the primary resource providing technical and regulatory expertise to the Councils.Presents findings and recommendations from internal and external audits to clinical departments and recommends solutions for implementing appropriate changes.Conducts internal reviews and provides quality review of external billing quality audits. Works with providers and department billing staff to address and resolve documentation deficiencies.Develops and implements Clinical Documentation Improvement Programs in partnership with the clinical departments.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Aug 07, 2024

Los Angeles, CA

|

Nurse

|

Perm

|

$55 - $60 (hourly estimate)

{"JobID":373242,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-118.424090909091,"Longitude":34.0819090909091,"Distance":null},"State":"California","Zip":"90095","ReferenceID":"HFL-724741","PostedDate":"\/Date(1723022085000)\/","Description":"ONSITE AT THE HOSPITAL The Admissions RN is a registered nurse and an Interdisciplinary Team member whose primary responsibility is to present VITAS services and philosophy to patients and families in a manner that results in the admission of appropriate patientsParticipation in the information gathering, analysis, education and form completion aspects of the admissions processEvaluate patients for hospice appropriateness, e.g. medical records review as requestedObtain agreement for admission of referred patients and families who meet admission criteriaAnalyze data collected by the LPN to facilitate/obtain admission ordersBuild effective referral source relationships to support the high quality and responsiveness expectations associated with VITASMaintain clinical and professional competenceTake the initiative in developing effective relationships internally with the appropriate admissions and patient care resource personsUtilize interpersonal skills to help appropriately educate and address any questions the patient and/or patient\u0027s family has concerning hospice and palliative careWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Admissions RN- LA","City":"Los Angeles","ExpirationDate":null,"PriorityOrder":0,"Requirements":"1 Year clinical rn expRN LICENSE IN CA","Skills":"icuhospice","Industry":"Nurse","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":60.0000,"SalaryLow":55.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

ONSITE AT THE HOSPITAL The Admissions RN is a registered nurse and an Interdisciplinary Team member whose primary responsibility is to present VITAS services and philosophy to patients and families... in a manner that results in the admission of appropriate patientsParticipation in the information gathering, analysis, education and form completion aspects of the admissions processEvaluate patients for hospice appropriateness, e.g. medical records review as requestedObtain agreement for admission of referred patients and families who meet admission criteriaAnalyze data collected by the LPN to facilitate/obtain admission ordersBuild effective referral source relationships to support the high quality and responsiveness expectations associated with VITASMaintain clinical and professional competenceTake the initiative in developing effective relationships internally with the appropriate admissions and patient care resource personsUtilize interpersonal skills to help appropriately educate and address any questions the patient and/or patient's family has concerning hospice and palliative careWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 06, 2025

Pittsburgh, PA

|

Data Warehousing

|

Contract-to-perm

|

$30 - $37 (hourly estimate)

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As a Data Analyst, he/she will gather requirements, create and maintain data extraction processes, and analyze patterns or trends in complex datasets. You will interpret results to provide... stakeholders with clear, data-driven insights that address current business questions, support investments, product development lifecycles, and other critical business needs. Working in a fast-paced and evolving environment, you will collaborate with cross[1]functional teams, prioritize multiple projects, and help ensure that analytical best practices are consistently applied. You will work alongside a multidisciplinary team of business, technical, and clinical professionals to deliver quality data insights supporting either the Digital, Translational or Clinical Trials business unit.Additional responsibilities: Gather Requirements: Work with stakeholders to clarify project objectives, discover data sources, and document needs. Data Querying & Profiling: Write moderate-to-advanced SQL queries to extract relevant information from diverse databases. Data Cleaning & Validation: Identify and remediate data quality issues, ensuring the accuracy and integrity of results. Pattern Identification: Use statistical or basic scripting methods (e.g., Python) to detect trends or anomalies in datasets. Reporting & Visualization: Produce dashboards, slide decks, or other visual reports summarizing analytical findings for stakeholder presentations. Translate Business Questions: Communicate effectively with non-technical and technical audiences to clarify needs and align on key analytical goals. Present Insights: Summarize and present results through clear, concise visuals and written narratives, ensuring stakeholders can readily understand the business impacts. Collaborative Engagement: Work in partnership with Product Managers, Clinicians, and other Data Analysts to refine data solutions that fulfill project objectives. Independent Project Management: Plan and monitor tasks and timelines for your projects using tools such as Jira, escalating risks and constraints to leadership as needed. Cross-Functional Collaboration: Contribute to team meetings, agile ceremonies, and milestone reviews, offering input on improving data workflows or identifying new data sources.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

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