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Associate Weekend Clinical Research Jobs (NOW HIRING)

Tribe Clinical Research

Clinical Research Coordinator

Greer, SC · On-site

$23.25 - $31/hr

Clinical Research Coordinator Position: Full-Time, Hourly Based at: TCR - Greer Position Summary ... Collaboration with QA * Trains other clinical trial associates making sure all individuals are up ...

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IMA Clinical Research, Inc.

$60 - $65/hr

Clinical Research Coordinator - Clinical Trials IMA Clinical Research | Chicago, IL Full-Time | ... A predictable schedule -- no nights, weekends, or on-call requirements The IMA Group is an ...

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As of Sep 2, 2026, the average hourly pay for associate weekend clinical research in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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Associate Weekend Clinical Research jobs near you

Clinical Research Coordinator

FIDES clinical research

Sandy Springs, GA • On-site

$24 - $32/hr

Other

Posted 2 days ago

New

Job description

Company Description FIDES Clinical Research is a dedicated clinical research organization focused on conducting high-quality clinical trials that advance medical knowledge and improve patient care. The team collaborates with sponsors, healthcare professionals, and participants to ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards. FIDES Clinical Research emphasizes data integrity, participant safety, and clear communication throughout the research process. The organization offers a professional environment where clinical research staff can develop their skills and contribute meaningfully to the progress of new therapies and treatments.
Role Description This is a full-time, on-site Clinical Research Coordinator role based in Sandy Springs, GA. The Clinical Research Coordinator will manage day-to-day study activities, including screening and enrolling participants, scheduling study visits, and maintaining accurate source documentation and case report forms. Responsibilities include coordinating informed consent discussions, ensuring adherence to study protocols, handling regulatory submissions, and maintaining study files. The role involves close collaboration with investigators, sponsors, monitors, and site staff to ensure compliance with Good Clinical Practice (GCP) and institutional policies. The coordinator will also track study timelines, report adverse events, and support data entry, query resolution, and overall study quality.
Qualifications
  • Experience with informed consent processes and participant education, ensuring ethical and compliant enrollment.
  • Strong understanding of study protocols and ability to implement protocol requirements accurately in daily study operations.
  • Solid research skills, including data collection, documentation, and use of electronic data capture systems.
  • Demonstrated clinical research experience, preferably in coordinating clinical trials in outpatient or site-based settings.
  • Familiarity with clinical trials conduct, Good Clinical Practice (GCP), and regulatory guidelines (FDA, IRB).
  • Excellent organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
  • Effective written and verbal communication skills for interacting with participants, investigators, monitors, and sponsors.
  • Ability to work on-site in Sandy Springs, GA, and collaborate within a multidisciplinary clinical research team.
  • Proficiency in basic computer applications and electronic medical record (EMR) or clinical trial management systems is beneficial.
  • Associate or bachelor’s degree in a health-related field, life sciences, or equivalent experience in clinical research is preferred.

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