Research documentation jobs

The Clinical Research Coordinator II is responsible for day-to-day coordination of interventional Phase I-III clinical trials and observational Cancer Control studies, overseeing subject-level study workflows from screening to data reporting.

Compensation

The hourly pay range for this position is from $32.63 to $48.93 and pay offered will be based on experience and qualifications.

Responsibilities

Conduct daily clinical operations of assigned research studies in accordance with study protocols, regulatory and GCP guidelines, and institutional policy.
Develop and maintain tools for study implementation, including data collection tools, reference materials, and specific study orders.
Provide study-specific education and training to clinic staff, participants, and other stakeholders.
Coordinate patient enrollment and participation by reviewing study candidates' medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.
Schedule patient clinic visits and ongoing study visits; ensure administrative compliance with study protocols.

Requirements

High school diploma or equivalent
Associate's or bachelor's degree in a healthcare, life sciences, public health, or related field
Nice to have: Certified Clinical Research Coordinator (CCRC)
Nice to have: Certified Clinical Research Professional (CCRP/SOCRA)
Nice to have: Experience working with NIH, FDA, OHRP, and ICH-GCP regulations

Research Assistant I

Research Assistant I

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Senior UX Researcher, Patient & Provider Experience

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Clinical Research Coordinator II

Compensation

Responsibilities

Requirements

Skills

Benefits