Clinical Research Coordinator (Nashville) Job at Medasource, Nashville, TN

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  • Medasource
  • Nashville, TN

Job Description

Position: Clinical Research Coordinator I

Client: Large Healthcare Organization

Location: Onsite - Nashville, TN

Duration: 1-year contract - possibility of FTE conversion

MUST RESIDE IN NASHVILLE OR NEARBY

Position Summary:

The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.

Major Responsibilities:

  • Oncology and Infectious Disease / Pediatric Oncology
  • Practice and adhere to the Code of Conduct philosophy and Mission and Value Statement
  • During your employment you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
  • Performs routine operational activities for multiple research protocols
  • Liaise between site research personnel, industry sponsors, and Supervisor
  • Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
  • Coordinates schedule of assessments from initial submission of feasibility until study closeout
  • Reviews the study design and inclusion/exclusion criteria with physician and patient
  • Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
  • Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
  • Creates study specific tools for source documentation when not provided by sponsor
  • Collects, completes, and enters data into study specific case report forms or electronic data capture systems
  • Generates and tracks drug shipments, device shipments, and supplies as needed
  • Ensures timely and accurate data completion
  • Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
  • Communicates all protocol-related issues to appropriate study personnel or manager
  • Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
  • Reviews and responds to any monitoring and auditing findings

Qualifications:

  • Bachelor's degree - Required
  • 1+ years of relevant experience - Required
  • Phlebotomy - Required
  • Certified Clinical Research Coordinator - Preferred

Job Tags

Contract work, Part time, Local area,

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