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Senior Clinical Research Coordinator

1 month ago

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

Vitalief is seeking a highly skilled Senior Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating and managing clinical trials, ensuring compliance with regulatory requirements, and providing exceptional patient care.

Key Responsibilities
  • Coordinate and manage clinical trials, including patient screening, consent, and data collection.
  • Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) and Institutional Review Board (IRB) guidelines.
  • Collaborate with research staff, investigators, and sponsors to ensure timely and efficient trial execution.
  • Develop and maintain research records, including patient consent forms, case report forms, and study documentation.
  • Participate in site preparation, including protocol feasibility, study budget development, and IRB application preparation.
Requirements
  • Bachelor's degree in a life science or related field.
  • Minimum of 2 years of experience in clinical research, with a focus on patient recruiting, screening, and retention.
  • Strong knowledge of GCP and IRB guidelines.
  • Excellent communication and organizational skills.
  • Ability to work independently and as part of a team.
What We Offer
  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.