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Clinical Research Organizer information

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$49K

$107.3K

$189K

How much do clinical research organizer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical research organizer 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 organizer?

A Clinical Research Organizer is a professional responsible for coordinating, planning, and managing the logistics of clinical research studies. They ensure that clinical trials are conducted efficiently, ethically, and according to regulatory requirements. Their duties often include scheduling study visits, maintaining study documentation, managing participant recruitment, and serving as a liaison between research teams and stakeholders. Clinical Research Organizers play a crucial role in ensuring that research projects run smoothly and reach their objectives within set timelines.

What are the key skills and qualifications needed to thrive as a clinical research organizer, and why are they important?

To thrive as a Clinical Research Organizer, you need strong project management skills, a background in life sciences or healthcare, and a solid understanding of clinical trial protocols and regulatory requirements. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are often expected. Exceptional organizational skills, attention to detail, and effective communication help you coordinate study teams and manage timelines. These skills are crucial for ensuring compliance, maintaining data integrity, and driving successful clinical research outcomes.

What are some common challenges faced by clinical research organizers when coordinating multi-site studies?

Clinical Research Organizers often encounter challenges in maintaining consistent communication and data management across multiple study sites. Differences in site procedures, varying levels of staff experience, and adherence to protocols can lead to discrepancies or delays. To address these issues, organizers typically implement standardized processes, conduct regular check-ins, and use centralized data systems. Strong organizational and interpersonal skills are essential for ensuring smooth collaboration and study compliance across all locations.

What cities are hiring for Clinical Research Organizer jobs?

Cities with the most Clinical Research Organizer job openings:

What states have the most Clinical Research Organizer jobs?

States with the most job openings for Clinical Research Organizer jobs include:

What are popular job titles related to Clinical Research Organizer jobs?

For Clinical Research Organizer jobs, the most frequently searched job titles are:

Infographic showing various Clinical Research Organizer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Metairie, LA • On-site

Prolerity Clinical Research
See more jobs at Prolerity Clinical Researchexternal

Full-time

Re-posted 28 days ago

Job description

Description:

The Clinical Research Assistant (CRA) assists in the daily activities of clinical research studies and clinic operations. This role involves working closely with clinical teams, investigators, and study participants to ensure that all required procedures and visits occur according to protocol-specific guidelines.

Key Responsibilities:

  •  Study Familiarization: Thoroughly understand assigned studies by reading protocols, attending start-up meetings, and coordinating with the Principal Investigator and study team.
  •  Protocol Adherence: Ensure strict adherence to study protocols and obtain exemptions when applicable.
  •  Specimen Collection & Processing: Collect, process, and ship laboratory samples in accordance with study requirements.
  •  Patient Screening & Qualification: Collect initial psychiatric and medical information through patient interviews and access appropriate sources to qualify and accurately place patients in enrolling clinical trials.
  •  Study Coordination Support: Assist Clinical Research Coordinators in trial-related organization and documentation, including filing and maintaining regulatory records.
  •  Communication & Reporting: Communicate protocol issues to the study team, Site Administrator, Principal Investigator (PI), or Sub-Investigator as needed.
  •  Clinical Tasks: Perform clinical tasks such as vital signs measurement, height and weight recording, ECG administration, phlebotomy, and specimen packaging.
  •  Documentation & Compliance: Maintain timely source documentation and ensure compliance with sponsor-required information.
  •  Patient Education: Educate patients and their families about study participation and clinical drug trials in general.
  •  Community Engagement: Assist in community outreach events and provide appropriate community resource referrals to patients, caretakers, and family members when applicable.
  •  Additional Duties: Perform ad-hoc tasks and assist in other study-related activities as needed.

Additional Responsibilities:

This job description outlines the primary responsibilities of the Clinical Research Assistant; however, additional duties may be assigned as needed to support the research program or the operational needs of the organization. These additional responsibilities are not limited to the above and may evolve over time based on study requirements or business needs.

Requirements:

Knowledge, Skills, and Abilities:

  •  Communication: Ability to communicate effectively (both written and oral) with patients, study teams, and external stakeholders.
  •  Interpersonal Skills: Excellent interpersonal and customer service skills to engage with study participants and colleagues.
  •  Organizational Skills: Strong ability to prioritize tasks, manage multiple responsibilities, and maintain documentation.
  •  Technical Proficiency: Proficiency in Microsoft Office software required; knowledge of Electronic Medical Records (EMR) systems preferred.
  •  Attention to Detail: High level of accuracy in maintaining documentation and following protocol guidelines.
  •  Team Collaboration: Ability to work independently and collaboratively within a multidisciplinary team.
  •  Confidentiality: Ability to handle sensitive participant data while adhering to ethical and regulatory guidelines.

Required Experience and Qualifications:

  •  Education: Bachelor’s degree preferred.
  •  Experience: Previous experience in a healthcare or clinical research setting is a plus.
  •  Clinical Trials Knowledge: Previous exposure to clinical trials is preferred but not required.

This role is ideal for someone detail-oriented, organized, and eager to support clinical research in advancing medical knowledge and patient care.