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Clinical Operations Associate Jobs in Durham, NC

IQVIA

Associate Director, Clinical Operations

Durham, NC · On-site

$97K - $270K/yr

IQVIA is seeking an Associate Director, Clinical Operations: Job Overview Direct a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and ...

ICON

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring ...

Icon plc

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring ...

ICON

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring ...

Icon plc

Clinical Operations Specialist

Raleigh, NC · On-site

Clinical Operations Specialist ICON is a global healthcare intelligence and clinical research ... As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring ...

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Clinical Operations Associate information

See Durham, NC salary details

$10

$23

$48

How much do clinical operations associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical operations associate in Durham, NC is $23.78, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $27.45 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Durham, NC?

The most popular types of Clinical Operations jobs in Durham, NC are:

What are popular job titles related to Clinical Operations Associate jobs in Durham, NC?

For Clinical Operations Associate jobs in Durham, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Durham, NC look for?

The top searched job categories for Clinical Operations Associate jobs in Durham, NC are:

What cities near Durham, NC are hiring for Clinical Operations Associate jobs?

Cities near Durham, NC with the most Clinical Operations Associate job openings:

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Durham, NC as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $52,749 per year, or $25.4 per hour.

Manager, Clinical Operations

410 ICR United States USA

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Manager, Clinical Operations

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.


As a Manager, Clinical Operations at ICON, you will oversee the execution of clinical trials, ensuring that they are conducted efficiently, on time, and in compliance with regulatory requirements.

What You Will Do:

Your focus will be on coordinating clinical operations delivery, resolving issues, and developing team capability.
Key responsibilities include:

  • Leading the operational planning and execution of clinical trials, ensuring adherence to protocols and timelines.
  • Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the clinical development process.
  • Monitoring trial progress and performance metrics, providing insights to inform decision-making and drive continuous improvement.
  • Mentoring and developing junior staff, fostering a culture of collaboration and excellence within the team.
  • Building strong relationships with internal and external stakeholders to facilitate smooth communication across clinical operations.

Your Profile:

You will have solid clinical operations experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Experience in managing clinical teams, with a solid understanding of Clinical Research Associate requirements
  • Clinical Research Associate experience required
  • Strong leadership skills with the ability to motivate teams effectively in a dynamic environment.
  • Proficiency in project management tools and methodologies, with a keen focus on optimizing processes.
  • Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes.
  • Willingness to travel as required (approximately 30%)

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