About The Position

The Senior Clinical Research Associate performs on-site or remote pre-study, initiation, interim, and close-out monitoring visits to ensure investigational sites and staff remain adequate for study conduct. The role verifies that investigators have the qualifications, resources, facilities, equipment, and staff needed throughout a clinical study. It also includes training site staff, supporting regulatory or ethics committee submissions when applicable, and mentoring or co-monitoring with new and junior staff.

Requirements

  • College or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
  • Extensive on-site monitoring experience in Phase 2/3 trials.
  • Full working proficiency in English.
  • Ability to plan, multitask, and work in a dynamic team environment.
  • Communication, collaboration, and problem-solving skills.
  • Ability to travel nationally.

Nice To Haves

  • Experience with complex trials in oncology or rare disease.

Responsibilities

  • Perform on-site or remote pre-study, initiation, interim, and close-out monitoring visit activities.
  • Ensure investigational site facilities and staff remain adequate for the conduct of the study.
  • Identify investigators and verify their qualifications, resources, facilities, equipment, and staff for the duration of the study.
  • Train investigational site staff as necessary.
  • Support preparation of regulatory and/or ethics committee submissions when applicable.
  • Mentor and train new staff, including conducting co-monitoring visits to assess junior staff performance.
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