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How much do clinical research organization jobs pay per year?

As of Aug 23, 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, 15% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Nurse Practitioner

Monroe Biomedical Research

Louisville, KY • On-site

Other

Medical, Dental, Vision

Posted 16 days ago

Job description

MBR - Louisville, KY | Onsite
ABOUT THE ROLE
Monroe Biomedical Research is growing, and we are seeking an experienced, patient-focused Clinical Research Nurse Practitioner to join our Louisville team.
This unique role combines advanced clinical practice with hands-on clinical research coordination. The Clinical Research Nurse Practitioner will work directly with study participants while supporting the successful execution of clinical trials from patient screening and study visits through documentation and follow-up.
This is an excellent opportunity for an NP who enjoys direct patient care, thrives in a fast-paced clinical environment, and is interested in contributing to research that advances medicine and expands treatment options for patients.
WHAT YOU'LL DO
Clinical Research & Study Management
• Coordinate and manage clinical trial visits from screening through study completion
• Review study protocols and ensure required procedures and assessments are completed accurately and within protocol-defined timelines
• Develop and maintain accurate and complete source documentation in accordance with study protocols
• Support participant screening, enrollment, and ongoing study activities
• Work closely with investigators, sponsors, monitors, and internal research staff to support successful study execution
• Ensure clinical trials are conducted in accordance with Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and internal procedures.
Patient Care & Clinical Responsibilities
• Provide clinical assessment and care to adult study participants within the scope of NP practice and study protocol requirements
• Perform and/or oversee study-related clinical procedures, including blood draws, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments
• Review relevant medical history, medications, laboratory results, and other clinical information
• Educate participants regarding study requirements, procedures, medications, and follow-up expectations
• Identify and communicate changes in participant condition, adverse events, or other clinically significant findings to appropriate study team members
• Provide a professional, compassionate, and supportive experience throughout each participant's clinical trial journey.
Data, Documentation & Quality
• Review and process medical records and study-related clinical documentation
• Accurately document study visits and clinical findings
• Enter and maintain study data in sponsor and clinical research systems accurately and within required timelines
• Prepare, process, and coordinate shipment of laboratory specimens according to protocol requirements
• Respond to data queries and assist with maintaining complete, inspection-ready study records
QUALIFICATIONS
• Current Nurse Practitioner (NP) licensure with the ability to practice with an adult patient population
• Master's degree in Nursing or related advanced practice field required
• Previous experience providing direct patient care required
• Clinical research experience strongly preferred
• Strong clinical judgment and commitment to patient safety
• Excellent attention to detail, organization, and documentation skills
• Ability to interpret and follow detailed clinical trial protocols
• Ability to effectively manage competing priorities and multiple studies in a fast-paced research environment
• Strong communication and interpersonal skills with a patient-centered approach
WHY JOIN MONROE BIOMEDICAL RESEARCH?
• Join a growing clinical research organization contributing to the advancement of new treatments and therapies
• Work alongside a collaborative and supportive multidisciplinary research team
• Gain exposure to a diverse portfolio of clinical trials
• Opportunity to combine advanced clinical skills with clinical research experience
• 100% company-paid employee Health, Dental, and Vision insurance

Apply