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Associate Director Clinical Research Jobs in Raleigh, NC

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and ...

IQVIA

Clinical Research Associate

Durham, NC · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

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All JobsAssociate Clinical Research JobsAssociate Director Clinical Research JobsAssociate Director Clinical Research Jobs in Raleigh, NC

Associate Director Clinical Research information

See Raleigh, NC salary details

$27.1K

$149K

$287.6K

How much do associate director clinical research jobs pay per year?

As of Aug 21, 2026, the average yearly pay for associate director clinical research in Raleigh, NC is $148,988.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,274.00 and $188,966.00 per year, depending on experience, location, and employer.

What does an associate director clinical research do?

An Associate Director of Clinical Research is responsible for overseeing the planning, execution, and management of clinical trials within a pharmaceutical or biotechnology company. They ensure that all research activities comply with regulatory requirements, company policies, and ethical standards. Their role often includes supervising clinical project teams, managing budgets and timelines, and liaising with external partners such as contract research organizations (CROs) and regulatory agencies. Additionally, they play a key part in developing clinical study protocols, monitoring trial progress, and ensuring data integrity for successful drug development.

What are the key skills and qualifications needed to thrive as an associate director clinical research?

To thrive as an Associate Director Clinical Research, you need advanced knowledge of clinical trial design, regulatory compliance, and drug development, typically supported by a relevant advanced degree and significant industry experience. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and familiarity with GCP and FDA/EMA regulations are crucial. Strong leadership, strategic thinking, and excellent communication skills help build effective teams and manage complex projects. These skills ensure successful, compliant clinical trials that advance organizational goals and safeguard patient safety.

What are some typical challenges faced by an associate director clinical research when leading cross-functional teams?

As an Associate Director of Clinical Research, you may encounter challenges such as aligning priorities across diverse functional groups (e.g., regulatory, data management, and clinical operations), managing tight timelines, and ensuring clear communication among stakeholders. Navigating regulatory requirements and adapting to evolving study protocols also require strong problem-solving skills. Success in this role often depends on your ability to foster collaboration and maintain focus on project goals while balancing the needs of multiple departments.

What is the difference between Associate Director Clinical Research vs Clinical Project Manager?

AspectAssociate Director Clinical ResearchClinical Project Manager
CredentialsTypically requires a PhD, MD, or advanced degree in life sciences; relevant certifications like RAC or CCRP are commonBachelor's or master's degree in life sciences or related field; certifications like PMP are advantageous
Work EnvironmentLeads multiple clinical trials, oversees teams, and collaborates with senior management in pharmaceutical or biotech companiesManages specific clinical trials, coordinates teams, and ensures project milestones are met within clinical research settings
Employer & Industry UsageUsed in pharmaceutical, biotech, and CROs for senior clinical research leadership rolesCommonly employed in pharmaceutical companies and CROs for trial management

The Associate Director Clinical Research typically holds a higher strategic and leadership role, overseeing multiple projects and teams, whereas the Clinical Project Manager focuses on the day-to-day management of individual clinical trials. Both roles require strong knowledge of clinical research processes, but the Associate Director often has more seniority and broader responsibilities.

What are popular job titles related to Associate Director Clinical Research jobs in Raleigh, NC?

For Associate Director Clinical Research jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Associate Director Clinical Research jobs in Raleigh, NC look for?

The top searched job categories for Associate Director Clinical Research jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Associate Director Clinical Research jobs?

Cities near Raleigh, NC with the most Associate Director Clinical Research job openings:

Associate Director Clinical Research jobs near you
Infographic showing various Associate Director Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $148,988 per year, or $71.6 per hour.

Director, Clinical Research Scientist

410 ICR United States USA

Raleigh, NC

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

New

Job description

Director, Clinical Research Scientist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What You Will Do:

  • Development of protocols for clinical studies. 

  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans. 

  • Drafting of clinical scientific documents such as IND, IND amendments, Clinical Study Reports, Investigator Brochures, Annual Reports, and other health authorities submissions. 

  • Responsible for providing clinical input into eCRF design, SAP, and TLFs. 

  • Monitor, review, and summarize clinical safety and efficacy data in ongoing studies. 

  • Collaborate with study team members to conduct timely and thorough review of study data using best practices and available tools to identify and evaluate data trends. 

  • Will lead the clinical matrix teams for assigned studies, represent clinical development on project teams and serve as liaison to project teams, CRO's and others. 

  • Provide clinical updates on assigned studies to Sr. management, Project Teams, Joint Project Teams and/or Steering Committees (if appropriate), Clinical sub-teams, internal strategy, and governance meetings, eDMC meetings, steering committees, advocacy groups, scientific advisory boards, and publications committees. 

  • Liaise with cross functions on training of current studies, results, meeting with lead PIs/KOLs at conferences; present as needed. 

  • Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design. 

  • Contribute to writing and review of study abstracts, posters, oral presentations, and manuscripts for assigned studies. 

Your Profile:

  • Degree in scientific/life-sciences field. Pharm.D. or Ph.D. preferred. 

  • Minimum of 4 - 6 years of experience in research with at least 3 or more years of clinical research/drug development experience are required for Director level. 

  • Experience in Immunology field is required.

  • Ability to multi-task and work in a fast-paced environment. 

  • Excellent written and oral communication skills. 

  • Strong Analytical ability. 

  • Ability to accommodate up to 20% travel or as business dictates. 


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply