Clinical Trials Data Management Jobs

The Gastroenterology Therapeutic Area Lead role within US Medical Affairs at Johnson & Johnson focuses on leading scientific strategy and business planning for immunology and gastroenterology assets. The position involves supervising a matrixed team to design evidence generation strategies, oversee Phase 3b and 4 clinical trials, and collaborate with global functions including R&D and commercial teams. Key responsibilities include managing budget decisions, serving as a subject matter expert for regulatory and publication activities, and mentoring direct reports. This leadership opportunity appeals to professionals seeking to drive breakthrough treatments for complex immune diseases within a mission-driven culture. The role is based in Horsham, Pennsylvania, operating on a hybrid schedule with three days in the office and two days remote, requiring up to 25 percent travel.

This Clinical Research Associate role at ICON plc supports the Utah-based team in managing investigational sites across the southeast region. The position involves serving as the primary liaison between sites and sponsors, conducting various site visits including initiation and monitoring, and ensuring strict compliance with ICH-GCP regulations. Key responsibilities include maintaining accurate documentation in clinical systems, monitoring patient safety data, resolving data queries, and overseeing drug accountability. The role appeals to professionals seeking a career in a world-leading healthcare intelligence organization that fosters an inclusive culture, rewards high performance, and offers comprehensive benefits focused on well-being and work-life balance. Candidates must be willing to travel up to 50% for on-site monitoring visits.

The Clinical Development Scientist Manager role supports scientific oversight and data integrity for Internal Medicine clinical trials within a global pharmaceutical team. Key responsibilities include contributing to protocol development and amendments, reviewing safety data and adverse events, managing clinical data quality, and supporting regulatory submissions and audits. The position offers the opportunity to work on pivotal Phase 3 studies in cardiometabolic diseases while collaborating with cross-functional teams and external stakeholders. This hybrid role provides a dynamic environment focused on continuous process improvement and innovative trial execution, with potential for global travel to support study sites and investigator meetings.

This Lead Clinical Research Coordinator role at ProPharma involves managing and coordinating daily activities for Phase II-III industry-sponsored clinical trials from initiation to close-out. The position requires ensuring protocol compliance, data integrity, and participant safety while handling vendor management, subject recruitment, adverse event reporting, and regulatory documentation. Key responsibilities include performing clinical procedures like phlebotomy, leading monitoring visits, and collaborating with investigators and sponsors to optimize study operations. The role is appealing for its opportunity to work with a diverse team in a culture that values innovation, diversity, and authentic collaboration. While the position requires residency in New York City, it offers a hybrid work arrangement that balances remote flexibility with in-person office collaboration.

The Clinical Scientist role within Merz Aesthetics Research and Development supports the global clinical strategy for aesthetic products and devices. Key responsibilities include designing clinical trials, authoring regulatory documents such as study protocols and clinical investigation reports, and interpreting data to support product registration. The position involves collaborating with cross-functional teams to manage external vendors and ensure compliance with international regulations. This opportunity appeals to professionals seeking to contribute to a family-owned company with a mission to enhance confidence through aesthetic medicine. The role offers a dynamic environment focused on scientific innovation and professional growth within a collaborative global team.

This full-time Clinical Research Assistant role supports the Cancer Institute at Memorial Regional Medical Center within the Bon Secours organization. The position assists the research team with administrative and financial operations, including patient enrollment in studies, managing regulatory documents for IRB submissions, and handling billing inquiries through Epic and ConnectCare systems. Key responsibilities involve maintaining trial archives, preparing for audits, and ensuring accurate data collection while upholding patient privacy. The role appeals to candidates seeking a mission-driven environment that values compassion and collaboration, offering opportunities for professional growth through tuition assistance and continuing education. The position is based on-site during day shifts with a standard 40-hour work week.

This Senior Manager role within the Oncology Clinical Development team provides scientific oversight for clinical trials supporting the company's cancer treatment portfolio. Key responsibilities include ensuring data integrity and quality, authoring critical regulatory documents such as protocols and informed consent forms, and leading data review strategies to analyze emerging safety profiles. The position involves collaborating with cross-functional partners to drive study execution and presenting findings to governance bodies. The role is appealing for its opportunity to contribute directly to patient care through impactful oncology research, offering a collaborative environment that values innovation and global perspectives. This hybrid position requires on-site presence approximately 2.5 days per week.

The Associate Director of Treasury role at BridgeBio leads global treasury operations for a biopharmaceutical company focused on developing life-changing medicines for rare diseases. Reporting to the Chief Accounting Officer, the position provides strategic oversight of cash liquidity, financial risk management, and banking relationships across commercial, R&D, and manufacturing functions. Key responsibilities include managing rolling cash flow forecasts for clinical trials and milestone payments, executing hedging strategies for foreign exchange and interest rate exposure, and optimizing the global bank account structure. The role appeals to candidates who value a mission-driven culture that encourages experimentation and the ethical use of AI to drive efficiency. It offers a hybrid work arrangement, opportunities to mentor a high-performing team, and a collaborative environment where professionals can influence executive strategy while supporting the rapid advancement of the pharmaceutical pipeline.

The Regional Medical Director for Austin provides clinical leadership and oversight across Mission Pet Health's veterinary network in the region. This role involves setting medical standards, developing clinical protocols, and mentoring veterinarians to ensure high-quality patient care. Key responsibilities include partnering with operations leaders to align medical goals with business growth, managing workforce planning and talent development, and utilizing data metrics to drive continuous improvement. The position offers a hybrid work arrangement with travel across the Austin area, allowing for both in-hospital presence and strategic remote work. It is particularly appealing for those seeking to shape the future of veterinary medicine within an innovative culture that values collaboration, science-based approaches, and the well-being of pets and their families.

The Product Analyst II role at Sarah Cannon Research Institute supports digital transformation within a leading oncology research organization. The position serves as a bridge between business stakeholders and IT teams to drive operational excellence and data integrity. Key responsibilities include gathering requirements, building AI-enabled prototypes, translating strategy into user stories, and ensuring compliance with clinical research regulations. This opportunity appeals to mission-driven professionals seeking to advance cancer treatment outcomes through hands-on delivery and rapid experimentation. The role emphasizes continuous learning and the application of emerging digital capabilities in a collaborative, fast-paced environment.

The Regulatory Associate role supports oncology clinical trials at UNC LCCC by ensuring strict adherence to federal regulations and Good Clinical Practice. Key responsibilities include preparing and submitting regulatory applications to the IRB and various committees, drafting informed consent forms, and managing compliance tracking for assigned disease groups. The position also involves preparing for audits, maintaining electronic regulatory binders, and contributing to process improvements through standard operating procedures and team mentoring. This opportunity appeals to candidates seeking to advance their expertise in clinical research compliance within a mission-driven environment focused on patient safety and research integrity. The role requires occasional evening or weekend availability and offers a collaborative setting for professional growth in a specialized oncology research department.

This part-time faculty role combines clinical nursing with education at the Barbara Davis Center for Childhood Diabetes within the University of Colorado Anschutz Medical Campus. The position focuses on providing care to children and adults at risk for or in early stages of type 1 diabetes. Key responsibilities include administering infusion therapies, conducting oral glucose tolerance tests, and delivering comprehensive diabetes education to patients and families. The role also involves contributing to ongoing clinical research protocols and navigating patient care within a multidisciplinary team. This opportunity is appealing for its unique blend of direct patient care, academic instruction, and involvement in cutting-edge immunotherapy research. The position is onsite in Aurora, Colorado, with a flexible schedule that includes occasional weekend coverage.

This full-time onsite role at the Cleveland facility serves as the primary point of contact for clinical investigator sites, pharmaceutical sponsors, and laboratories within the Biospecimen Operations team. The position focuses on maintaining rigorous quality control standards by reviewing critical documents, resolving data errors, and managing client communications via phone and email. Key responsibilities include operating specialized clinical trials management software, tracking sample requisitions, and training new employees. The role appeals to candidates seeking a collaborative environment where strong organizational skills and adaptability are valued, offering the opportunity to support high-stakes medical research while working a standard weekday schedule.

The Sr. Director or Vice President of Finance role serves as a strategic executive partner to the CEO and Board at Supira Medical, a clinical-stage medical device company developing ventricular assist devices. Key responsibilities include building financial infrastructure for U.S. pivotal trials, leading AICPA-compliant reporting and internal controls, managing capital strategy and investor relations, and overseeing the selection and implementation of a first integrated ERP system. The position also involves scaling the finance organization to support the transition from pre-revenue to commercial operations. This opportunity appeals to leaders seeking to shape the financial future of an innovative life sciences firm, offering the chance to build systems from the ground up while contributing to a mission that addresses critical cardiology needs.

The Oncology Nurse Navigator role involves a registered nurse guiding patients and families through the entire cancer care continuum, from diagnosis to survivorship or end-of-life care. Key responsibilities include coordinating diagnostic testing and treatments, providing disease-specific education, and advocating for patients to overcome medical, financial, and logistical barriers. The position requires collaboration with a multidisciplinary team to ensure timely, high-quality care while tracking program metrics. This opportunity appeals to nurses seeking a patient-centered environment that values compassion, collaboration, and respect. The role is based in outpatient cancer centers or clinics with standard business hours and emphasizes care coordination over physical patient lifting.

This part-time summer internship places candidates within the Corporate Social Responsibility and Strategic Operations departments of a major nonprofit health system. The role involves supporting community engagement initiatives, conducting data analysis on program impact, and assisting with project coordination and stakeholder reporting. Interns will also manage meeting logistics and contribute to process documentation while collaborating with a dedicated cohort. The position offers a hybrid or remote work arrangement with flexibility to accommodate academic schedules. It is particularly appealing for students seeking hands-on experience in a mission-driven environment that prioritizes community health and strategic growth, providing exposure to professional tools and organizational best practices.

The Associate Director, Succession and Assessment Strategy role leads enterprise-level frameworks for leadership continuity and workforce sustainability within Bristol Myers Squibb's talent organization. Key responsibilities include designing succession planning strategies for critical roles, managing executive assessment and coaching programs, and utilizing Workday analytics to provide visibility into leadership readiness and risk. The position appeals to professionals seeking to drive meaningful impact on patient care through strategic talent development while partnering with senior leadership. The role offers a collaborative culture focused on innovation and inclusion, with a hybrid work arrangement requiring at least 50% onsite presence in Princeton, New Jersey.

This full-time Medical Physicist role supports the expansion of the OhioHealth Radiation Oncology team across multiple care sites in Columbus, Ohio. The position involves providing clinical physics support for complex treatments such as SBRT, SRS, and brachytherapy, while managing quality assurance programs and equipment commissioning. Key responsibilities include ensuring regulatory compliance, developing new treatment techniques, and collaborating with a large team of physicists and dosimetrists. The role offers a hybrid work environment with opportunities for remote chart checks and participation in clinical trials. Candidates are drawn to the supportive culture that values lifelong learning and excellence, the chance to work with advanced technology, and the ability to contribute to a systemwide network of care sites.

The Pharmacy Technician IV role within the Research Pharmacy department at the University of Arkansas for Medical Sciences serves as a lead technician supporting investigational drug services. Key responsibilities include managing inventory, preparing sterile and non-sterile investigational products, maintaining detailed clinical trial records, and ensuring compliance with USP standards. The position also involves educating pharmacy students and training new employees. This opportunity is appealing for its collaborative culture focused on advancing healthcare research, comprehensive benefits including retirement matching and education discounts, and the chance to work in a diverse, mission-driven academic medical center.

This part-time per diem Registered Nurse role is based in the Emergency Department at Atrium Health Carolinas Medical Center. The position involves assessing patient conditions, administering treatments, and collaborating with interdisciplinary teams to deliver evidence-based care across the continuum of treatment. Key responsibilities include maintaining accurate electronic health records, participating in quality improvement initiatives, and ensuring a culture of safety within a fast-paced clinical environment. The role appeals to nurses seeking flexible scheduling in a dynamic setting, offering opportunities for professional development and exposure to diverse patient populations. Candidates will work within a large, nationally recognized health system known for clinical innovation and a commitment to equitable care.

The Assistant Director, Business Administrator role within the University of Cincinnati Department of Surgery supports operations and finance for a top-tier medical department. Key responsibilities include managing departmental budgets, overseeing financial reporting and variance analysis, supervising administrative staff, and ensuring compliance with grants and clinical trial contracts. The position appeals to candidates seeking a mission-driven environment where they can contribute to a leading academic health system's tripartite mission of education, research, and patient care. The role offers a collaborative culture with significant opportunities for professional development, robust retirement plans, and a comprehensive benefits package including tuition remission and generous paid time off. This is an on-site position within a university setting.

This field-facing Medical Science Liaison role within Sanofi's R&D team focuses on the Dupilumab dermatology portfolio across Southern California, Nevada, and Hawaii. The position serves as a trusted scientific partner to key opinion leaders and healthcare providers, conducting one-on-one and group exchanges to advance understanding of the disease state and product value. Key responsibilities include developing stakeholder engagement strategies, gathering medical insights to inform future research, and supporting evidence-generation activities such as investigator-led studies. The role appeals to candidates seeking to drive medical innovation at the forefront of AI-powered drug discovery while contributing to a mission that improves lives globally. The position offers a supportive culture with significant opportunities for career growth and requires a valid driver's license for regional travel.