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Per Diem Clinical Research information

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How much do per diem clinical research jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for per diem clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a per diem clinical research?

A Per Diem Clinical Research job is a flexible, as-needed position in which professionals support clinical research studies without a fixed schedule. These roles typically involve assisting with patient enrollment, data collection, regulatory compliance, and study monitoring. Per diem employees work on an on-call basis, meaning their hours depend on study needs. This position is ideal for those looking for flexibility while contributing to clinical trials.

What are the typical work hours and scheduling expectations for a per diem clinical research role?

Per Diem Clinical Research professionals usually work on an as-needed basis, which offers significant flexibility but can also mean unpredictable hours. Assignments may vary depending on ongoing clinical trials, site needs, or specific phases of research, and shifts could include weekdays, weekends, or evenings. This flexible structure is ideal for those seeking to balance other commitments or gain diverse research experience across multiple studies or clinical environments. Team collaboration is often coordinated around study timelines, making effective communication especially important. Being comfortable with varying workloads and adapting quickly to new protocols is key to thriving in this dynamic role.

What are the key skills and qualifications needed to thrive in the per diem clinical research position, and why are they important?

To succeed as a Per Diem Clinical Research professional, you typically need a background in life sciences or health-related fields, strong attention to detail, and experience with research protocols. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and Good Clinical Practice (GCP) certification is often expected. Excellent organizational skills, effective communication, and adaptability are crucial soft skills for working in variable settings and teams. These competencies help ensure compliance, data integrity, and seamless collaboration in fast-paced and flexible clinical research environments.

Can you make good money in per diem clinical research?

Per diem clinical research roles can offer competitive pay rates, often higher than full-time positions due to their temporary or flexible nature. Earnings depend on factors such as experience, certifications, and the number of assignments, with some professionals earning a substantial income through multiple shifts. However, income can vary widely based on location and demand for clinical trials.

Is a Per Diem Clinical Research a good career?

A Per Diem Clinical Research role involves temporary or flexible work in clinical trial settings, often requiring knowledge of Good Clinical Practice (GCP) and regulatory guidelines. It can offer flexibility and diverse experience but may lack consistent income and benefits compared to full-time positions. This career path is suitable for those seeking part-time work or additional experience in clinical research.
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What are the most commonly searched types of Clinical Research jobs?

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What states have the most Per Diem Clinical Research jobs?

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Per Diem Clinical Research jobs near you
Infographic showing various Per Diem Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

PER DIEM CLINICAL RESEARCH COORDINATOR

Doral, FL • On-site

SRA Trials
See more jobs at SRA Trialsexternal

$30/hr

Per diem

Posted 4 days ago

Job description

Suncoast Research Associates is a privately owned and operated research organization established in 2018. We help volunteers get involved in clinical trials, which allow patients to play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research. Our company works with all major pharmaceutical companies and conducts studies in a myriad of therapeutic areas. We are located in Doral, Florida.
We are seeking a reliable, detail-oriented Per-Diem Clinical Research Coordinator to support daily clinical trial operations at our investigative site. The ideal candidate has a strong working knowledge of GCP/ICH guidelines, study protocol procedures, and site-level workflows. This role provides supplemental support during high-volume periods, subject visits, monitoring visits, and other operational needs.
Key Responsibilities
  • Assist with conducting study visits, including preparing visit materials, room setup, and subject flow management.
  • Perform source documentation, data entry, and eDiary/ePRO troubleshooting in accordance with protocol and GCP.
  • Maintain accurate, timely documentation in source, eCRF/EDC systems, CTMS, and regulatory binders as required.
  • Assist with specimen collection, processing, packaging, and shipment per study-specific lab manuals (phlebotomy experience preferred).
  • Support coordinators with tracking AE/SAE documentation, conmed changes, and protocol-mandated assessments.
  • Facilitate monitoring visits by assisting with data clarification, document retrieval, and query resolution.
  • Maintain study supplies, inventory logs, and temperature monitoring documentation.
  • Contribute to subject recruitment efforts, including prescreening, chart review, and outreach follow-up.
  • Ensure compliance with SOPs, protocol procedures, ICH-GCP, and site quality standards.
Qualifications
  • Minimum 3 years of hands-on clinical research experience.
  • Strong understanding of ICH-GCP, FDA regulations, and protocol adherence.
  • Proficiency with EDC platforms, CTMS, IWRS/RTSM systems, and ePRO/eDiary troubleshooting.
  • Ability to perform accurate documentation, multitask effectively, and work independently with minimal supervision.
  • Excellent communication, professionalism, and attention to detail.
  • Phlebotomy experience strongly preferred (but not required).
  • Bilingual English/Spanish is a plus.
Work Expectations
  • Must be available to work on an as-needed basis, including flexibility to support varying schedules based on study and operational needs.
  • Ability to quickly become familiar with study-specific protocols, procedures, and site workflows.
  • Provide coverage and operational support to the clinical research team as needed based on site workload and scheduling demands.
  • Assist with preparation for sponsor, CRO, and regulatory monitoring visits or audits, as applicable.
  • Escalate protocol deviations, safety concerns, data discrepancies, or other study-related issues to the appropriate site personnel.
Join our team as a Per Diem Clinical Research Coordinator and play a critical role in supporting our research team. Apply today!

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