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Temporary Research Participants Jobs (NOW HIRING)

University of Miami

Research Assistant 1

Miami, FL

$18.50 - $25.25/hr

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Obtain informed consent and ensure that participants fully understand the research procedures.

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Temporary Research Participants information

Can you get paid for participating in research studies?

Temporary research participants are often compensated for their time and effort, with payment amounts varying depending on the study's complexity and duration. Compensation can be in the form of cash, gift cards, or other incentives, and participants may need to meet specific eligibility criteria or complete training before taking part.
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Infographic showing various Temporary Research Participants job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution.

Research (Professional)

University of Pittsburgh

Pittsburgh, PA • On-site

Full-time

Re-posted 8 days ago

Job description

The Academic Research Center for Hematology (ARCH) at the University of Pittsburgh is seeking a Temporary Clinical Research Coordinator to support clinical research focused primarily on sickle cell disease and other hematological disorders. This role plays a key part in the coordination and execution of investigator-initiated and industry-sponsored clinical studies.
Core Responsibilities:
• Study Coordination: Coordinate day-to-day activities for clinical research studies, including study startup, participant visits, data collection, and study closeout.
• Participant Engagement: Support recruitment, screening, informed consent, scheduling, and retention of research participants.
• Data & Documentation: Maintain accurate study documentation, enter data into study databases, and ensure timely query resolution. Assist with study finance tracking
• Regulatory & Compliance: Assist with IRB submissions, protocol amendments, adverse event reporting, and ensure compliance
• Team Collaboration: Work closely with investigators, clinical staff, sponsors, and research team members to support high-quality, patient-centered research.

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