Upsilon Global

Contract Clinical Trial Associate/Clinical Research Coordinator

4 days left

United States
Hourly Rate ($40-65)
12 Apr 2021
12 May 2021
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Contract Clinical Research Coordinator - 100% Capacity - Mid-Sized CRO - Early Phase Oncology

Upsilon Global are currently looking for an experienced Contract Clinical Research Coordinator on behalf of one of our specialist CRO partners. Working within a small team, you’ll be supporting the clinical department with administration for essential documents as well as clinical trial support in a wider context. Being a small organisation, you’ll have the opportunity to experience a wider range of responsibility than typical larger organisations, with great progression potential for your career if you’re looking to progress into a CRA capacity.

Experience as a CRC is essential, along with the ability to self-motivate and self-manage as this is a home-based position.


Details confidential, information available upon request. Specialist oncology CRO with major expansion plans in the US, wider Europe and APAC. Extremely well respected, based on a long-standing reputation of high-quality delivery in highly scientific protocols with a range of exciting pharmaceutical sponsors.

Main Responsibilities

  • Administration, identification and filing of crucial documents for TMF to assist with inspection readiness for pivotal studies.
  • Prepare site for monitoring
  • Administration and clinical trial support (supplies, documentation, assistance to Quality management team and other ad-hoc tasks)
  • To create and maintain Project Documents and TMF (Trial Master Files) in accordance to ICH-GCP.
  • If required, you will be asked to accompany Clinical project manager and research associate on site visits.
  • To attend, prepare and take minutes of regular project meetings


  • Previous CRC experience of 3 years' minimum
  • Excellent demonstration of communication skills, including an ability to ensure that important information is consistently shared with managers, peers, team members, and business partners in a timely manner and an ability to facilitate functional team meetings
  • Demonstration of proactivity and initiative, including reliably delivering on assignments and demonstrating a willingness to receive feedback and course correct.

Other skills and abilities

  • The ability to communicate effectively in English
  • Good computer literacy with working knowledge of PCs, Windows and Microsoft Office
  • Willingness to support the clinical team

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