Upsilon Global

Senior CRA - Netherlands - Home-Based

07 Jan 2021
06 Feb 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Home-Based Senior CRA – Netherlands

Upsilon Global are working closely with a mid-sized, US-based, Global CRO, who have recently increased their European presence as a result of a merger with an Eastern European CRO as they are looking to build a clinical study team of Senior CRAs in the Netherlands.

They are operational in a wide range of countries across Europe including the UK, Germany and Italy, and are looking to cement their clinical operations within The Netherlands through the growth of their small but growing team in The Netherlands

This expanding CRO conduct studies in a wide range of therapeutic areas including Oncology and Rare Disease, as well as Cardiology studies and will offer you the opportunity to work on the full cycle of a clinical trial from regulatory submissions and site feasibility, through to study close-out and database lock. This allows each and every CRA to develop their skills much further than a CRA in a larger CRO, setting you up for Project Management in the future!


Details confidential, information available upon request. Specialist mid-sized CRO establishing a presence in The Netherlands and seeking people looking to join them on their development journey. You’ll be a crucial member of this growing department and the progression opportunities and endless.

Main responsibilities

  • 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-IV clinical trials across The Netherlands
  • 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

  • A BSc or BA degree in a lifescience related field
  • Minimum of 4-5 years independent monitoring experience
  • Sound knowledge of ICH/GCP and regulatory requirements
  • Experience using clinical trial management systems

Other skills and abilities

  • The ability to communicate effectively in English and Dutch
  • Good computer literacy with working knowledge of PCs, Windows and Microsoft Office
  • Full capabilities to drive in The Netherlands
  • Regulatory experience strongly desired

Salary and Benefits

  • Competitive salary
  • Home-based role
  • Great opportunities for career progression
  • Fantastic company culture and cross-functioning teams and departments

For further information on this opportunity and to learn of similar positions, please contact Upsilon Global on +44. (0). 20. 3. 87. 5.  99. 66. or email ‘applications (at) upsilonglobal . com’


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