Upsilon Global

Clinical Research Associate – Permanent – USA

7 days left

United States
$110-$125,000 per year
21 May 2021
20 Jun 2021
CHKLS- 101
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Upsilon Global are currently seeking a SCRA based in the USA, for one of our long-standing partners. Our partner a mid-sized CRO which is a specialist within oncology and rare diseases, mainly focusing on phases I/II working closely with small biotech’s and mid-sized sponsors. The CRO has grown by 300% over the last 3 years and is continuing to grow.

Currently they are expanding their team in the US and are seeking a motivated, driven and team player SCRA to join the team in a home-based position.

Main responsibilities

  • Would be doing both monitoring and submission work.
  • Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
  • To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required
  • Ensure that all study related communication including e-mail is tracked, printed, and filed as required
  • The set-up and coordination of Phase I-II
  • To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA
  • To liaise with all other appropriate departments to ensure the smooth running of the study
  • Mentor and train other CRA’s as and when required
  • Perform document submissions to local authorities
  • To assemble files and ensure documents for the trial master file accurately reflect the progress of the study
  • Other Ad-Hoc CRA duties

Education and Qualifications

  • University Degree/College degree in life sciences or similar.
  • Experience in phases I/II is preferred.
  • Minimum 5 years of oncology experience.
  • Minimum 5 years of CRA experience.
  • Ability to travel nationwide. 60-70% travel.
  • Remote and risk-based monitoring experience.
  • Oncology experience 3 years or more
  • Desired experience in submissions.

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