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$107.3K

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How much do clinical research organization jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical research organization in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a clinical research organization?

A Clinical Research Organization (CRO) job involves supporting pharmaceutical, biotechnology, and medical device companies in conducting clinical trials and research. CRO employees help with tasks such as regulatory compliance, data management, patient recruitment, and trial monitoring. These roles ensure that new treatments and medical advancements are tested safely and efficiently. Positions within a CRO can range from clinical research associates to data analysts and project managers. Working in a CRO offers opportunities to contribute to drug development while collaborating with sponsors and regulatory agencies.

What are the key skills and qualifications needed to thrive in a clinical research organization position?

To excel within a Clinical Research Organization, individuals typically need a background in life sciences, strong project management skills, and experience with clinical trial protocols and regulatory requirements. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication enhance collaboration across multidisciplinary teams and with sponsors. These skills are crucial for maintaining compliance, ensuring data integrity, and delivering successful clinical research projects.

What kinds of career growth opportunities are available when working for a clinical research organization?

Clinical Research Organizations (CROs) offer a range of career advancement opportunities across clinical operations, data management, regulatory affairs, and project management. Employees often start in entry-level roles such as Clinical Research Associate (CRA) or Data Coordinator and can progress to senior, management, or specialist positions with experience and further training. CROs frequently support professional development through training programs and encourage movement between departments, allowing for a diverse and rewarding career path. Teamwork, adaptability, and a proactive approach to skill-building are key to seizing growth opportunities in this dynamic industry.

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Clinical Research Organization jobs near you
Infographic showing various Clinical Research Organization job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator

FIDES clinical research

Sandy Springs, GA • On-site

$24 - $32/hr

Other

Posted 3 days ago

New

Job description

Company Description FIDES Clinical Research is a dedicated clinical research organization focused on conducting high-quality clinical trials that advance medical knowledge and improve patient care. The team collaborates with sponsors, healthcare professionals, and participants to ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards. FIDES Clinical Research emphasizes data integrity, participant safety, and clear communication throughout the research process. The organization offers a professional environment where clinical research staff can develop their skills and contribute meaningfully to the progress of new therapies and treatments.
Role Description This is a full-time, on-site Clinical Research Coordinator role based in Sandy Springs, GA. The Clinical Research Coordinator will manage day-to-day study activities, including screening and enrolling participants, scheduling study visits, and maintaining accurate source documentation and case report forms. Responsibilities include coordinating informed consent discussions, ensuring adherence to study protocols, handling regulatory submissions, and maintaining study files. The role involves close collaboration with investigators, sponsors, monitors, and site staff to ensure compliance with Good Clinical Practice (GCP) and institutional policies. The coordinator will also track study timelines, report adverse events, and support data entry, query resolution, and overall study quality.
Qualifications
  • Experience with informed consent processes and participant education, ensuring ethical and compliant enrollment.
  • Strong understanding of study protocols and ability to implement protocol requirements accurately in daily study operations.
  • Solid research skills, including data collection, documentation, and use of electronic data capture systems.
  • Demonstrated clinical research experience, preferably in coordinating clinical trials in outpatient or site-based settings.
  • Familiarity with clinical trials conduct, Good Clinical Practice (GCP), and regulatory guidelines (FDA, IRB).
  • Excellent organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
  • Effective written and verbal communication skills for interacting with participants, investigators, monitors, and sponsors.
  • Ability to work on-site in Sandy Springs, GA, and collaborate within a multidisciplinary clinical research team.
  • Proficiency in basic computer applications and electronic medical record (EMR) or clinical trial management systems is beneficial.
  • Associate or bachelor’s degree in a health-related field, life sciences, or equivalent experience in clinical research is preferred.

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