Part-Time Clinical Research Coordinator
Must Haves: Must have previous experience in Clinical Research and have inputted Data into EDC system.
Hours: 16 hours per week, between days and times of Monday-Friday 8am-5pm. The site is flexible to whichever days work best for your schedule. This is an ONSITE position.
Contract Duration: 3 month contract
Benefits: No benefits offered since this is a part-time role.
Role & Responsibilities:
- May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO
- Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol
- Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol
- Collects, verifies, organizes and records clinical information and data in electronic data capture systems (EDC). Abstracts data from necessary sources to complete the EDC and resolve queries.
- Performs the following data related activities: EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding
- May be responsible for regulatory submissions.
- Need working knowledge of essential documents and IRB requirements
- Participates in site feasibility determination, site qualification visits, site initiation visits and research related meetings
- May be responsible for recruiting clinical trials to site
- May have patient contact
Job Description:
- Data Entry into EDC platforms
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