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Clinical Trial Manager Jobs in Raleigh, NC (NOW HIRING)

Clinical Trial Manager Our client, a leading organization in clinical research, is seeking a dedicated Clinical Trial Manager to join their team. As a Clinical Trial Manager, you will be an integral ...

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start-up, site management and monitoring activities. This includes vendor management ...

At least two years of experience in clinical study management, clinical operations, or related clinical trial roles. * Experience working with CROs, vendors, clinical sites, and cross-functional ...

At least two years of experience in clinical study management, clinical operations, or related clinical trial roles. * Experience working with CROs, vendors, clinical sites, and cross-functional ...

Author and manage essential trial documentation including protocols, informed consent forms (ICFs ... Manage and mentor clinical operations staff, including performance appraisals, development planning ...

Author and manage essential trial documentation including protocols, informed consent forms (ICFs ... Manage and mentor clinical operations staff, including performance appraisals, development planning ...

Demonstrated ability to lead and manage global clinical teams in a matrix structure, delegate ... trial management systems. • Language Skills: Fluent in English. • Core Competencies:

As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What ...

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Clinical Trial Manager information

See Raleigh, NC salary details

$28

$60

$93

How much do clinical trial manager jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for clinical trial manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.28 and $68.46 per hour, depending on experience, location, and employer.

What does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

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

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

What are the most commonly searched types of Clinical Trial jobs in Raleigh, NC?

The most popular types of Clinical Trial jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Trial Manager jobs?

Cities near Raleigh, NC with the most Clinical Trial Manager job openings:

Infographic showing various Clinical Trial Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $126,397 per year, or $60.8 per hour.

Clinical Trial Manager

Experis

Chapel Hill, NC • On-site

Other

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago


Job description

Clinical Trial Manager

Our client, a leading organization in clinical research, is seeking a dedicated Clinical Trial Manager to join their team. As a Clinical Trial Manager, you will be an integral part of the Clinical Operations department supporting project teams. The ideal candidate will demonstrate strong leadership, excellent organizational skills, and effective communication.

Location: Chapel Hill, NC

Pay Range: 58.26-64.00 per hour

What's the Job?
  • Manage all clinical operational and quality aspects of allocated studies, ensuring compliance with ICH GCP standards.
  • Develop and implement clinical tools such as Monitoring Plans and Guidelines, contributing to the Master Action Plan (MAP).
  • Coordinate study start-up activities, including ethics and regulatory submissions, ensuring timely and accurate documentation.
  • Lead and motivate clinical teams, ensuring project timelines, resources, and quality standards are maintained.
  • Monitor clinical trial progress, review monitoring visit reports, and manage data collection and query resolution to meet contractual obligations.
What's Needed?
  • Bachelor's degree or equivalent with relevant academic or vocational qualifications.
  • Minimum of 5+ years of experience in clinical trial management or related roles.
  • Strong knowledge of ICH GCP, FDA guidelines, and clinical monitoring practices.
  • Excellent leadership, planning, and organizational skills with the ability to adapt to changing environments.
  • Effective communication skills in English, both written and oral, with proficiency in using automated systems such as Outlook, Excel, and Word.
What's in it for me?
  • Opportunity to work on impactful clinical research projects in a dynamic environment.
  • Collaborative team culture that values diversity and inclusion.
  • Chance to develop your skills and advance your career within a reputable organization.
  • Supportive management committed to your professional growth.
  • Work in a location that fosters innovation and excellence in clinical research.

Upon completion of waiting period consultants are eligible for:

  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account
  • Health Flexible Spending Account
  • Dependent Care Flexible Spending Account
  • Supplemental Life Insurance
  • Short Term and Long Term Disability Insurance
  • Business Travel Insurance
  • 401(k), Plus Match
  • Weekly Pay