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MSD Clinical Research Associate 
Sweden, Stockholm 
771260107

24.11.2024

Job Description

As a CRA you will be part of a very engaged team ensuring excellent studies and high site performance. Clinical Research at the company is given top priority and is a cornerstone of the business. Consequently, you will as a CRA have considerable responsibility.

As a CRA you play an important part in ensuring performance and compliance with ICH/GCP and country regulations for assigned studies and sites. In your role you will act as the primary site contact and site manager, taking the overall responsibility of allocated sites.

Finally, as one of our fast-paced and resourceful CRA you will also be actively developing and expanding the territory for clinical research – including finding and developing new sites.

About you

Furthermore, we are looking for colleague that:

  • Is fluent in both Swedish and in English
  • Has good understanding and working knowledge of clinical research, phases of clinical trials, current ICH/GCP & country clinical research laws & guidelines
  • Is good at analyzing data and at seeing challenges where others might see a problem
  • Has a tolerant attitude and understanding for working in a multicultural setting
  • Has advanced IT-skills (Use of MS office, use of various clinical IT applications) and ability to adapt to new IT applications on various devices
  • Will be able to travel domestically and internationally approx. 50 percent of the working time
  • Has two years of experience with direct site management in pharma/bio/CRO
  • Holds a B.A./B.S. in Science and/or Biology
  • Holds a driver’s license

Current Contingent Workers apply


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