Freelance CRA for Orphan Drug trials in Europe

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Bedrijfsprofiel

Functie-eisen

PSR Orphan Experts is a full service CRO and the leading expert in assisting biotech and pharma companies with orphan drug development.
People living with a rare disease are at the center of everything we do at PSR. We focus on the rare disease patient, and how to make a positive impact on their lives. Our passion to work in the clinical research industry is to contribute to better health and effective treatments for patients suffering from serious diseases for which often no adequate treatment exists. That is why we are in this business.

  • At least 5+ years of CRA experience
  • Familiar with complex clinical trials (Orphan Drugs, Pediatrics, Oncology etc.)
  • Experience with local submissions
  • Highly proficient in spoken and written English
  • Extended GCP knowledge
  • Strong communication skills
  • Responsive
  • Pro-active
  • Hands-on mentality

Arbeidsvoorwaarden

Contract
  • FTE: 0,2 – 1,0
Arbeidsvoorwaarden
  • Dependent on project
Overig
  • Interesting Orphan Drug Projects!

Freelance CRA for Orphan Drug trials in Europe

Our CRO; PSR Orphan Experts is a full service CRO and the leading expert in assisting biotech and pharma companies with orphan drug development. PSR Orphan Experts is specialized in designing and executing complex clinical development programs requiring innovative regulatory and clinical approaches in both Europe and the US. In the end, at PSR we are all about making a positive impact on the lives of people with rare diseases.
PSR’s dedicated CRA’s will help to ensure that the studies are conducted smoothly, within the timelines and are very much aware of the importance of open and continuous communication. For different clinical trials in Orphan Diseases we are looking for experienced freelance CRA’s all across Europe (France, Belgium, Italy, Germany, Spain, United Kingdom) who could help us out in managing these Orphan Drug trials.

Are you a clinical professional with at least 5 years of CRA experience in a small Biotech, Pharma or small CRO company? Are you familiar with complex (phase 1,2) clinical trials (Orphan/Pediatric/Oncology etc.)? And do you have experience with local submissions in your country? Then we would like to get in touch!
Next to the desired professional profile, PSR also takes into account personality attributes, like a person’s communication style, in order to create the best possible match. Strong communication skills, giving your expert opinion, being pro-active and responsive, and managing expectations is very important in our opinion.

Let us know if you are interested in talking about freelance CRA opportunities (in France, Belgium, Italy, Germany, Spain, United Kingdom) through PSR’s Orphan Drug projects.

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