Research Operations Coordinator

1 week ago


New Brunswick, New Jersey, United States Vitalief Full time
Position: Clinical Research Coordinator at Vitalief

Why Join Vitalief?

Vitalief stands at the forefront of addressing healthcare workforce challenges. By becoming part of our team, you will significantly contribute to guiding clients through the dynamic realm of clinical research and trials with cutting-edge strategies.

About Us: At Vitalief, we are committed to nurturing the development and welfare of our team members, cultivating an environment rich in innovation and inclusivity.

Benefits of Being Part of Vitalief:

  • Focus on personal and professional growth through our PEOPLE FIRST ethos.
  • Promotion of creativity and teamwork – your input is valued.
  • Opportunities for mentorship with our skilled professionals to help you achieve your career aspirations.
  • Balanced work-life integration with generous paid time off and holidays, alongside comprehensive health and retirement plans.

Salary Range: $60,000 to $70,000 annually

Key Responsibilities:

  • Assisting in the management of Oncology clinical trials under the supervision of the Nurse Manager.
  • Facilitating patient screening, consent processes, activation, and care management.
  • Supporting the monitoring of patient appointments and data management.
  • Collaborating with healthcare professionals to ensure effective patient services.

Essential Qualifications:

  • 1-2 years of experience in Clinical Research, including patient management and data oversight.
  • Bachelor's Degree in a relevant discipline.
  • Experience in Oncology and complex clinical trials is advantageous.
  • Excellent organizational skills with the ability to manage multiple trials concurrently.
  • Proven adaptability and a positive mindset are crucial for success.
  • Familiarity with Good Clinical Practice (GCP) guidelines.
  • Experience with IRB submissions and reporting of Serious Adverse Events (SAEs).
  • Knowledge of EPIC and OnCore systems is beneficial.

Physical Requirements: Role involves standing, sitting, walking, and lifting up to 25lbs.

Additional Requirements: All on-site personnel must provide proof of Covid-19 vaccination, annual Influenza vaccination, and pass a Tuberculin Skin Test.



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