Clinical Research Study Manager

4 weeks ago


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

Vitalief is seeking a highly skilled Clinical Research Study Manager to join our team. As a key member of our clinical research operations team, you will be responsible for managing clinical research activities for various Oncology Phase 2 through 4 trials.

Key Responsibilities:

  • Provide support and establish workflows and processes to ensure high-quality clinical research activities.
  • Assure that all clinical research conducted is according to Good Clinical Practice (GCP) guidelines and applicable regulations.
  • Supervise clinical research staff, including training and guidance to ensure staff needs are met.
  • Develop and implement standard operating procedures to support the clinical research program.
  • Ensure clinical research processes are patient-centered.

Requirements:

  • Bachelor's Degree in a social science or related field.
  • 5 years of experience working in a clinical research institution.
  • 3 years of Oncology research experience.
  • One to two years of supervisory experience in a clinical research environment.
  • Association of Clinical Research Professional (ACRP) certification or Society of Clinical Research Associates (CCRP) certification required.

What We Offer:

  • Market-competitive salary based on experience level.
  • 20 PTO days plus 9 paid Holidays annually.
  • Company-paid life insurance and short/long-term disability coverage.
  • 401K retirement program.
  • Robust healthcare plans to choose from.

Work Environment:

Vitalief is a dynamic and innovative healthcare consulting company. Our team is passionate about empowering research and transforming clinical trials. We prioritize personal and professional growth for all employees and encourage innovation.

How to Apply:

Please submit your application, including your resume and cover letter, to [insert contact information].



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