Clinical Research Coordinator Job at Medix™, Nashville, TN

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  • Medix™
  • Nashville, TN

Job Description

6 month contract to full-time hire with company - paid weekly every Friday and benefits available after 30 days on contract.

Pay: $28-$33/hr based on years of experience and qualifications met

Mon-Fri 8-5 onsite

The client is looking for candidates with experience in:

  • 2 + years of coordinating clinical trials as CRC or RA
  • Multiple therapeutic areas expertise, Oncology a Plus+ (you will be working within the client's Oncology team so comfortable working with Oncology patients as well)
  • Patient facing experience, no remote CRC work

The position requires a Bachelor’s degree .

Key Responsibilities:

Patient-Facing Duties:

  • Serve as a primary point of contact for study participants, ensuring a positive and informed experience throughout their participation.
  • Assist with patient recruitment, screening, informed consent, and enrollment in oncology clinical trials.
  • Coordinate study visits, including scheduling, patient check-in, and preparation of required documentation.
  • Support research nurses and investigators during patient visits, including collection of vitals, specimen handling, and data recording (as permitted by scope and certification).
  • Communicate effectively with patients, families, and the clinical care team to facilitate adherence to study requirements.

Administrative & Research Support Duties:

  • Provide administrative support to the research nursing staff, including managing study binders, visit checklists, and data entry into electronic case report forms (eCRFs).
  • Maintain accurate and organized study documentation in compliance with Good Clinical Practice (GCP) and institutional SOPs.
  • Assist in preparing and submitting regulatory documents (IRB submissions, amendments, continuing reviews, etc.).
  • Track study supplies, ensure accurate specimen labeling/shipment, and manage inventory related to study conduct.
  • Coordinate communication between the clinical team, sponsors, and research office.
  • Participate in study meetings, site initiation visits, monitoring visits, and audits as needed.

Job Tags

Weekly pay, Full time, Contract work, Work at office,

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