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Study Management Associate Jobs in Raleigh, NC (NOW HIRING)

PSI CRO

Site Management Associate I

Durham, NC

Maintains study-specific and corporate tracking systems * Serves as the sites' primary contact point * Serves as the primary sites' contact point for vendors, study supplies, and access management

PSI CRO

Site Management Associate I

Durham, NC · On-site

Maintains study-specific and corporate tracking systems * Serves as the sites' primary contact point * Serves as the primary sites' contact point for vendors, study supplies, and access management

DRMP

Traffic Analysis Project Manager

Raleigh, NC · On-site

Oversee preparation of traffic engineering studies and traffic impact analyses through the life ... Supervises work of Project Managers, Associates, and Interns. * Responsible for personal ...

Duke University

Clinical Data Manager

Durham, NC · On-site

Associate's degree * Two years of relevant research experience. Completion of the DOCR North ... management operations to ensure the completion of requests made to the DAMT. Coordinate with study ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Assess and manage test article/study supply including supply, accountability, and destruction ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

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All JobsStudy Management Associate JobsStudy Management Associate Jobs in Raleigh, NC

Study Management Associate information

See Raleigh, NC salary details

$10

$39

$56

How much do study management associate jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for study management associate in Raleigh, NC is $39.01, according to ZipRecruiter salary data. Most workers in this role earn between $25.79 and $50.88 per hour, depending on experience, location, and employer.

What is a study management associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.

What are the typical responsibilities of a study management associate?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What are the key skills and qualifications needed to thrive as a study management associate?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are popular job titles related to Study Management Associate jobs in Raleigh, NC?

For Study Management Associate jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Study Management Associate jobs in Raleigh, NC look for?

The top searched job categories for Study Management Associate jobs in Raleigh, NC are:

Study Management Associate jobs near you
Infographic showing various Study Management Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $81,145 per year, or $39 per hour.

Associate Clinical Project Management Director, Immuno-oncology, IQVIA Biotech

NCBiotech

Durham, NC • On-site

$103 - $286/hr

Other

Posted 4 days ago

Job description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Join a team driving innovation in Immuno-Oncology and Cell & Gene Therapy clinical research. We are seeking an experienced Associate Clinical Project Management Director to lead the strategic planning, execution, and delivery of complex global clinical trials while ensuring exceptional quality, customer satisfaction, and financial performance.

Key Responsibilities

  • Lead and oversee global clinical studies and programs from start-up through closeout.
  • Serve as the primary contact for sponsors, building strong client relationships and providing strategic project leadership.
  • Drive study delivery by managing timelines, budgets, resources, risks, and quality outcomes.
  • Lead cross-functional teams to ensure operational excellence and successful milestone achievement.
  • Support business development activities, including proposal strategy and bid defense presentations.
  • Proactively identify and mitigate study risks, oversee issue resolution, and manage change control processes.
  • Mentor and develop project team members while fostering collaboration and continuous improvement.

Required Qualifications

  • Bachelor's degree in Life Sciences or a related field.
  • 10+ years of clinical research experience, including 6+ years of project management experience.
  • Direct experience in Immuno-Oncology and Cell & Gene Therapy clinical trials is required.
  • Strong knowledge of ICH-GCP, clinical trial regulations, and global study management.
  • Proven ability to lead cross-functional teams, manage sponsor relationships, and drive successful project delivery.
  • Excellent communication, leadership, financial management, and problem-solving skills.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $102,500.00 - $285,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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