Clinical Research Coordinator

4 weeks ago


New Brunswick, New Jersey, United States Vitalief Full time
Job Overview

Vitalief is a pioneering consultancy addressing the healthcare human capital epidemic. We are seeking a highly skilled Clinical Research Coordinator to join our team and contribute to the success of our clients in the research and clinical trial industry.

Key Responsibilities:

  • Manage eligibility check lists, perform patient screening/consenting, patient activation, and managing patient care.
  • Assist with monitoring patient visits, track deviations, and documenting SAEs.
  • Ship specimens to central labs or research labs, track data queries, and prepare data for audits.
  • Collaborate with team members to ensure coordinated services delivery to patients.

Requirements:

  • Minimum 1-2 years of experience in Clinical Research as a Clinical Research Coordinator.
  • Bachelor's Degree required.
  • Experience in Oncology and/or complex clinical trials is a plus.
  • Strong organizational and prioritization skills.
  • Considerable understanding of Good Clinical Practice (GCP) guidelines.

Why Work with Vitalief?

We offer a dynamic work environment, opportunities for growth and development, and a competitive salary range of $60,000 to $70,000 annually.

Work Environment:

Work is 5 days per week on-site in New Brunswick, NJ.

Important Note:

Vitalief requires all on-site resources to provide proof of full vaccination for Covid-19, annual influenza inoculation, and successful Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.



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