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How much do full time clinical research organization jobs pay per year?

As of Aug 20, 2026, the average yearly pay for full time 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 (CRO)?

A Clinical Research Organization (CRO) is a company that provides support to pharmaceutical, biotechnology, and medical device industries by offering research services outsourced on a contract basis. These organizations help manage and conduct clinical trials, handle regulatory affairs, data management, and ensure compliance with Good Clinical Practice (GCP). CROs play a crucial role in bringing new drugs and treatments to market more efficiently by streamlining the research process and reducing costs for sponsors. Full-time positions in a CRO can include roles in clinical operations, project management, data analysis, and quality assurance. Working in a CRO provides exposure to a variety of clinical trials and therapeutic areas.

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

Excelling in a Full-Time Clinical Research Organization role requires a solid background in life sciences, understanding of clinical trial protocols, and often a relevant degree such as in biology, pharmacology, or nursing. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are typically expected. Strong attention to detail, communication, and organizational skills help professionals effectively manage studies and collaborate with diverse stakeholders. These skills and qualifications are crucial for ensuring trial integrity, regulatory compliance, and successful research outcomes.

What are some common challenges faced when working full time at a clinical research organization (CRO)?

Working full-time at a Clinical Research Organization can be both rewarding and demanding. Common challenges include managing multiple studies simultaneously, adapting to evolving regulatory requirements, and meeting tight project deadlines. Team members often collaborate across departments—such as data management, regulatory affairs, and clinical operations—which requires strong communication and organizational skills. Navigating these challenges successfully provides valuable experience and opportunities for career growth within the clinical research field.

What cities are hiring for Full Time Clinical Research Organization jobs?

Cities with the most Full Time Clinical Research Organization job openings:

What are the most commonly searched types of Clinical Research Organization jobs?

The most popular types of Clinical Research Organization jobs are:

What states have the most Full Time Clinical Research Organization jobs?

States with the most job openings for Full Time Clinical Research Organization jobs include:

Full Time Clinical Research Organization jobs near you

Unblinded Clinical Research Coordinator II

DM Clinical Research

New York, NY • On-site

$26.50 - $35.25/hr

Full-time

Re-posted 9 days ago

Job description

Unblinded Clinical Research Coordinator II
DM Clinical Research is looking for an Unblinded Clinical Research Coordinator II to join our team in New Jersey. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required

Apply