Job Search Results for clinical research

Insight Global is seeking a Director of Clinical Research Operations to support a leading cardiovascular research program in Philadelphia. This individual will oversee daily clinical trial... More activities, guide research staff, and ensure compliance with FDA, GCP, and IRB standards. This person will manage study workflows, troubleshoot operational issues, coordinate regulatory needs, and support strategic growth of the Cardiovascular Clinical Research Unit. Strong leadership, clinical research operations expertise, and experience in academic or healthcare research settings are essential as this person will have 10 direct reports.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

PM Shift - 2:30pm-11pmThe Research Associate will collect face and body data gathered from large-scale capture domes and VR headsets by:?Staging and setting-up equipment for the study, which may... More include engaging with engineering, external equipment vendors, internal and external safety evaluators, and the research study team to ensure the equipment is set up properly. ?Conducting the study, including participant coaching and interaction, operating complex, experimental capture systems, and debriefing with team leadership as necessary?Performing basic troubleshooting of capture systems (hardware and software) and escalate any bugs or issues using internal tools.?Providing research study support, including data collection, tracking of participants, and tracking of equipment and procedures.?Contributing to and/or update existing documentation ?Serving as a participant for studies and being captured in various systems as needed.?Completing project work related to captures such as recording and updating capture scripts.?Attending all required trainings, meetings, and standups?Providing feedback for process improvement areasExpectations for Success To be able to successfully execute on the day-to-day responsibilities above, the Research Associate is expected to:?Review SOPs and other any other relevant documentation and consult with the responsible Lead for any questions or clarifications in advance of the capture.?Stay up to date with process and SOP changes for frequently used systems. ?Arrive on-time for captures and allow additional time, if needed, to review unfamiliar systems or SOPs and for operational set up?Arrive on-time and prepared with relevant information or materials for all required trainings, meetings, and standups.?Approach each capture and project with ability and flexibility. Be prepared to quickly pivot to new tasks, approaches to capture, or steps in documented processes to keep the team moving forward, even during blocking events.?Provide a comfortable and professional experience for participants (both internal and external) through all interactions including providing updates and breaks during troubleshooting or other capture-blocking events. ?Ensure highest quality and accuracy of data captured by maintaining a sterile and distraction-free capture environment.?Escalate any issues to the Engineer Team and properly documenting, in-detail, the nature of the issue.?Address any areas for improvement of the capture process in scheduled meetings and/or via internal feature request tools.?Identify (or partner with the Team Lead(s)) projects and tasks that can be completed during larger blocking events and during planned and unplanned system downtime.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

Insight Global is seek a Phase I Oncology Clinical Research Nurse at Hackensack Meridian Health. They will coordinate and manage early-phase clinical trials in a high-volume oncology clinic,... More requiring flexibility based on daily patient schedules and evolving protocol demands. This role balances direct patient care with complex research responsibilities, including screening and enrolling patients, presenting and obtaining informed consent, conducting protocol-driven assessments, triaging patient calls, managing data queries, and ensuring accurate, audit-ready documentation. Due to the nature of Phase I trials?where dosing schedules are adjusted and no established therapeutic dose exists?the nurse participates in teleconferences, reviews protocol amendments, supports dose-escalation processes, and collaborates closely with investigators, pharmacists, regulatory teams, and data coordinators to ensure patient safety and compliance. Candidates must have a strong oncology background (primarily solid tumor experience, some hematology exposure), be highly detail-oriented, and thrive in a fast-paced clinical research environment; Phase I experience is preferred, though broader oncology research experience will be considered.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

Insight Global is hiring for a Research Billing Specialist for one of our healthcare clients. Responsible for coordinating clinical trial billing, collection, and reconciliation, and supporting... More day-to-day department finance operations. The Research Billing Specialist invoices and tracks payments from clinical trial sponsors for patient visits and study costs according to budgets and contracts, reconciles payments to research accounts, and processes reimbursement requests for patients and third-party vendors in line with HMH policy. This role serves as a financial resource for clinical site staff and research patients, utilizes CTMS or financial software to monitor trial revenue, attends finance meetings, assists with account discrepancies, and prepares reports for the Finance department. Responsibilities also include troubleshooting billing processes, conducting billing training for staff and new hires, providing cross-coverage with the Research Billing Compliance Specialist by reviewing and transferring charges, preparing monthly reports, and maintaining DSA documentation. The specialist resolves outstanding patient bills and disputes, develops tracking metrics for research finance, maintains communication with ancillary departments and vendors, performs other assigned duties or projects, and adheres to HMH organizational competencies and standards of behavior.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

A Nationally Certified Comprehensive Cancer institute is seeking a Research Pharmacy Technician in the Investigational Drug Services (IDS) Pharmacy Department. This Research Pharmacy Technician... More supports the receipt and management of investigational inventory; as well as the preparation, labeling, and distribution of these products to help facilitate clinical trials research. This position will ensure compliance with regulatory standards and institutional protocols/standards are being followed at all times. Working under the supervision of a licensed pharmacist(s) within the research space, the technician will assist with the receiving (logging, labeling, and storing), transferring, and dispensing/ outpatient prescription processing of these investigational products. This technician will be tasked with communicating with Sponsors (i.e. drug companies) and Clinical Research Organizations for documentation, and collaboration, in conjunction with institutional research teams and providers. This role must uphold IDS Pharmacy standards at all times, in contributing to the overall quality and safety of patient care throughout all research patients at the institute. This is an exciting opportunity to join a well-established, gold-standard organization for Cancer Care!Compensation:$21/hr to $28/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401K retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.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 Human Resources Request Form. 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/ .Less

We are seeking a highly motivated Senior Scientist (Contract) to provide critical laboratory and scientific support for antibody?drug conjugate (ADC) programs during a period of temporary team... More coverage. This role will contribute directly to preclinical research efforts that inform clinical development decisions and support advancing oncology programs. This is a high impact, hands on role supporting a clinical stage oncology program. The position is time bound and intended to provide continuity and scientific excellence during planned team absences.The successful candidate will operate in a fast paced, collaborative research environment and work closely with internal cross functional partners as well as external contract research organizations (CROs). This is a high impact, hands on role supporting a clinical stage oncology program.Key Responsibilities?Design, execute, and support in vitro ADC related assays, including: oFlow cytometry based expression and target detection assaysoCytotoxicity (cytotox) assays?Analyze, interpret, and clearly communicate experimental data to support discovery and development objectives.?Collaborate cross functionally with scientists across Oncology Discovery to support program needs.?Interface with and support external CROs, including assay oversight, data review, and troubleshooting.?Maintain accurate experimental documentation and uphold scientific rigor, data integrity, and laboratory best practices.?Contribute to a collaborative, solution oriented team culture.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

Insight Global is seeking a Regulatory Specialist to join the Clinical Research team at Hackensack Meridian Health in Hackensack, NJ. This contract role will support compliance and regulatory... More operations for clinical trials, ensuring adherence to institutional, federal, and sponsor requirements. The Regulatory Specialist will be responsible for preparing, submitting, and maintaining regulatory documents such as IRB submissions, amendments, and continuing reviews, while ensuring compliance with FDA, ICH-GCP, and institutional policies. Additional duties include maintaining accurate regulatory files, tracking essential documents in CTMS, and communicating with sponsors, CROs, and internal stakeholders regarding regulatory requirements. The role also involves assisting with audits and inspections, implementing corrective actions, and supporting protocol activation and ongoing trial maintenance. Candidates should have a bachelor?s degree in life sciences or a related field (master?s preferred), at least 2?3 years of experience in clinical research regulatory affairs, and strong knowledge of IRB processes, FDA regulations, and GCP guidelines. Proficiency with CTMS and document management systems, excellent organizational and communication skills, and the ability to manage multiple studies and deadlines in a fast-paced environment are essential. This 40 hours a week, on-site position.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

The Demetris Research Histology Services (RHS) laboratory provides complete translational research histology services which include serving as a core lab for the Immune Tolerance Network (ITN),... More multiple Clinical Trials in Organ Transplantation (CTOT), and multiple grants and corporate local, national, and international clinical trials. The RHS lab specializes in sample preparation, sectioning, routine staining, and immunohistochemistry services. Currently, we are providing these services for twelve sponsors with additional contracts pending. Possible need for another lab technician to assist with the workflow and allow the lab to meet project requirements. Manages day-to-day laboratory operations while ensuring compliance with safety regulations and best practices. Works with, adapts, and installs scientific equipment in research laboratories. Develops and collaborates on routine projects and procedures. Manages inventory and equipment and performs budget functions. Essential Functions:?Must be able to perform all basic histology and immunohistochemistry procedures: grossing, processing, embedding, sectioning, special stains, equipment maintenance, other routine lab tasks?Follow established protocols and troubleshoot basic immunohistochemistry as necessary?Compliance with regulatory training and EHS requirements?Will be handling the entire lifecycleWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

Our large pharmaceutical client in Spring House, PA is seeking a Scientist to join the Decisional Analytics group within Cell Therapy API Development. This group is responsible for developing rapid,... More robust, and high-throughput analytical platforms to support multiple cell therapy programs, advancing them from early-stage development to late-stage clinical readiness. The successful candidate will leverage their technical expertise and experience to design, optimize, and execute assays to evaluate the attributes and quality of lentiviral vectors and CAR-T cell therapy processes and products, contributing to the cell therapy manufacturing platform. This is a unique opportunity to work within a cross-functional matrix environment supporting industry-leading autologous cell therapy programs that have made significant contributions to advancing human health and providing quality therapeutics to patients. Key Responsibilities:?Lead efforts within program teams to design, optimize, and execute bioanalytical methods for assessing lentiviral and cell therapy drug products during both process development and product testing.?Execute and optimize lentiviral vector characterization assays, including infectious titer, ELISA-based physical titer, MSD assay, residual host cell DNA and protein analysis, potency assays, and safety characterization through VCN assays.?Contribute to the development of novel, automated bioanalytical platforms to improve the efficiency and throughput of existing analytical assays.?Participate in routine lab operations, including lab maintenance, safety inspections, equipment maintenance, reagent qualifications, and other duties as required.?Analyze high-volume data and present research findings through written reports and oral presentations.?Collaborate with cross-functional teams, both internal and external (including contractors and different departments), to support the success of projects.?Lead or mentor other scientists on process, techniques, or tasks as needed.?Ensure data integrity and compliance with laboratory operations, including adherence to SOPs for data recording, equipment usage, and laboratory safety standards.?Maintain detailed, GxP-compliant records and notebooks, ensuring safety and environmental requirements are met.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less

A leading healthcare system is seeking a fully remote bilingual Project Coordinator to support community engagement, publication efforts, and cross-functional project delivery. This role serves as a... More central point of contact for stakeholders, managing project timelines, deliverables, and communications across multiple initiatives. The Project Coordinator will manage the National Community Engagement Group (NCEG) Publication Subcommittee, support manuscript development, and facilitate collaboration among researchers, patient caregivers, community partners, vendors, and internal design teams.This individual will help drive projects from concept to completion, ensuring alignment, compliance with regulations, and timely outcomes. Responsibilities include developing relationships with community partners, overseeing the creation of engagement toolkits and plain-language materials, facilitating manuscript kick-off calls, tracking progress, and resolving conflicts as needed. The role also supports the Associate Director with leadership tasks, NIH staff coordination, scheduling, and administrative support. Collaboration on summary videos and consultation on dissemination strategies are key components of the role. Proficiency with tools such as Calendly, SharePoint, Photoshop, and Doodle, along with comfort and trust in communicating with others, is essential.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, 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.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/.Less