Clinical Research Coordinator - 237307
: Job Details :


Clinical Research Coordinator - 237307

Medix™

Location: Rochester,NY, USA

Date: 2024-12-24T02:05:23Z

Job Description:

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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