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Clinical Trial Program Manager Jobs in Raleigh, NC

Jobtailor

Vice President, Clinical Development

Raleigh, NC · On-site

$180 - $260/hr

Clinical Trial Manager, Data Manager, Clinical Project Manager and Clinical Program Manager. * Personnel management of part‑time contractors who fill the roles of: biostatistician, Clinical Quality ...

Kite Pharma

Clinical Trials Manager

Raleigh, NC · On-site

$146K - $189K/yr

Monitors clinical trial sites. * Assists Clinical Program Manager in overall study management. * Drafts and coordinates review of relevant documents including protocols, informed consents, case ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

Referral program Summary: The Contract Clinical Study Manager provides operational leadership ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

Referral program Summary: The Contract Clinical Study Manager provides operational leadership ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC · On-site

Required Knowledge, Skills, and Abilities " Strong knowledge of clinical trial operations, study ... manage CROs, vendors, study timelines, risks, action items, and cross-functional deliverables ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

System One

Clinical Study Manager

Durham, NC · On-site

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

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All JobsClinical Trial Program JobsClinical Trial Program Manager JobsClinical Trial Program Manager Jobs in Raleigh, NC

Clinical Trial Program Manager information

See Raleigh, NC salary details

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How much do clinical trial program manager jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical trial program manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What does a clinical trial program manager do?

A Clinical Trial Program Manager oversees the planning, execution, and completion of clinical trials within an organization. They coordinate cross-functional teams, manage timelines and budgets, ensure compliance with regulatory guidelines, and maintain the quality and integrity of clinical data. Their role is essential for the successful development of new medical treatments, as they bridge communication between stakeholders, monitor progress, and address any issues that arise during trials.

What are some common challenges faced by clinical trial program managers, and how can they be addressed?

Clinical Trial Program Managers often encounter challenges such as managing complex timelines, coordinating multiple stakeholders, and ensuring regulatory compliance across different study sites. These challenges can be addressed by implementing robust project management tools, maintaining clear and consistent communication with cross-functional teams, and staying updated on regulatory requirements. Developing strong organizational skills and fostering collaborative relationships with investigators, sponsors, and regulatory bodies are also key to overcoming obstacles in this role.

What are the key skills and qualifications needed to thrive as a clinical trial program manager, and why are they important?

To thrive as a Clinical Trial Program Manager, you need strong project management skills, a background in life sciences or healthcare, and experience with clinical research regulations such as GCP, often supported by a relevant degree and certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory submission tools is typically required. Exceptional leadership, communication, and problem-solving abilities help you coordinate teams and manage complex stakeholder relationships. These skills ensure that clinical trials are conducted efficiently, compliantly, and successfully, leading to reliable study outcomes and regulatory approval.
What are popular job titles related to Clinical Trial Program Manager jobs in Raleigh, NC? For Clinical Trial Program Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Program Manager jobs in Raleigh, NC look for? The top searched job categories for Clinical Trial Program Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Trial Program Manager jobs? Cities near Raleigh, NC with the most Clinical Trial Program Manager job openings:
Clinical Trial Program Manager jobs near you
Infographic showing various Clinical Trial Program Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Vice President, Clinical Development

Jobtailor

Raleigh, NC • On-site

$180 - $260/hr

Other

Posted 6 days ago

Job description

Responsibilities
  • Development of Clinical Development strategy for all internal and external (partnered through licensing) programs, including timeline and cost estimates, inclusive of pre‑approval and post‑approval label‑expansion studies.
  • Personnel management of full‑time employees who fill the roles of: Clinical Trial Manager, Data Manager, Clinical Project Manager and Clinical Program Manager.
  • Personnel management of part‑time contractors who fill the roles of: biostatistician, Clinical Quality Manager, Medical Writing, Bioassay development, preclinical development, pharmacokinetics, clinical monitor / medical director (MD).
Requirements
  • Strong scientific and clinical development background spanning small molecules and biologic development in a broad range of therapeutic areas, including CNS, oncology, cardiovascular, anti‑infectives, GI, obesity, respiratory, and rare diseases.
  • Strong understanding of 505(b)(2) and hybrid medicine approval pathways and the strategies to minimize approval requirements for clinical studies.
  • Strong operational background in leading and managing the timelines and Phase I‑IV clinical trials globally.
  • Strong communication skills and ability to lead and contribute to cross‑functional teams.
  • Strong interpersonal skills to support, mentor and manage a high‑performing team of experienced clinical development professionals and related part‑time contractors.
  • MD or Ph.D. in a basic or health‑related scientific discipline with related research and drug development experience, with an emphasis in late‑stage clinical development expertise (Preferred).
  • Strong understanding of Clinical Regulatory (FDA, MHRA, ICH) guidelines and requirements, Clinical Quality and GCP regulations (Preferred).
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