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Clinical Trials Manager Jobs (NOW HIRING)

Tango Therapeutics

Clinical Trials Manager

Boston, MA · On-site

CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...

Tango Therapeutics

Clinical Trials Manager

Boston, MA · On-site

CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...

Houston Methodist

The Manager Clinical Trials position monitors progress and performance of all projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other ...

Gilead Sciences, Inc.

Clinical Trials Manager

$133K - $172K/yr

May serve as a resource for others within the company for clinical trials management expertise. * Under general supervision, is able to examine functional issues from an organizational perspective.

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

The Clinical Trials Manager (CTM), Clinical Operations, coordinates the activities associated with the evaluation, initiation, and management of solid tumor oncology clinical trials. This position is ...

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How much do clinical trials manager jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for clinical trials manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What does a Clinical Trials Manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are the key skills and qualifications needed to thrive as a Clinical Trials Manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are some common challenges faced by Clinical Trials Managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.
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Clinical Trials Manager jobs near you

Clinical Trials Manager

Nemours Children's Hospital Orlando

Wilmington, DE • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Trials Manager

Nemours is seeking a Clinical Trials Manager. The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours Children's Hospital- Delaware. Managing both Hematology and Oncology Research Associates, this position will support the Moseley Institute in Delaware Valley. Collaborating with Research partners across multiple Nemours sites and Non-Nemours sites this leadership role will work in conjunction with the enterprise coalition for the Nemours Center for Cancer and Blood Disorders (NCCBD).

Essential Functions:

A. Strategic Planning and Development: 1. Meet with the medical staff and faculty on a regular basis to assess their needs pertaining to clinical trials research. 2. Develop goals and performance measures in conjunction with the medical faculty to ensure growth and development of the clinical trials program. 3. Meet regularly with the Associate Administrator Delaware to provide feedback on new initiatives, performance of on-going initiatives, and seek feedback for future programmatic development. 4. Assist with budget management of the clinical trials program in Delaware Valley B. Supervision and Oversight: 1. Supervise and coordinate the daily activities of the research coordinators and staff. 2. Provide guidance and oversight for submissions to scientific and ethical review committees. 3. Review new research protocols and ensure there is adequate and appropriate staffing for current and planned protocols.

4. Conduct interviews and make hiring recommendations. 5. Provide oversight, periodic review including rounding, and feedback to clinical trials staff. 6. Provide procedures for systematic record keeping, drug accountability, patient interactions, equipment tracking, and good clinical practices. 7. Provide pre-review prior to external audit or investigations. 8. Responsible for performance management of designated staff.

Requirements:

  • Masters degree preferred; Bachelors degree with appropriate experience may be acceptable.
  • BSN with active Delaware Nursing License preferred.
  • Five years of Clinical Research Coordinator experience or equivalent experience required, with a minimum of 5 years clinical pediatric experience. Pediatric Oncology Clinical Research experience preferred.

Nemours Children's Health is an internationally recognized pediatric health system serving more than 1.7 million patient encounters each year. We deliver care across six states through two freestanding children's hospitals Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.

Backed by the Nemours Foundation and Alfred I. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach focuses equally on prevention and treatment, partnering with communities to help every child thrive.

Inclusion and belonging guide our strategy and growth. We are committed to culturally relevant care, reducing health disparities, and fostering an environment where every associate, patient, and family feels supported and valued.

Job Identification 18497

Job Category Clinical Support Staff

Posting Date 05/15/2026, 05:25 PM

Degree Level Bachelor's Degree

Job Schedule Full time

Locations 1600 Rockland Road, Wilmington, DE, 19803, US (On-site)

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