Clients

Client testimonials:

Read what some of our other clients have had to say about CK Clinical.

"CK Clinical is a pharmaceutical recruiter that has a great talent to match candidates to specific clients' needs. Jonathan and his group are easy to communicate with, honest and efficient but never pushy or "into your face". I have had a very good experience with the candidates that came through CK Clinical so I am planning to continue a relationship with CK Clinical for staffing needs that we have in the future." Biogen Idec

“CK Clinical - a really helpful and friendly company; always deliver what they promise and represent great value!” Sanofi-Aventis

"CK clinical were excellent at selecting candidates for us to view for our position. Not only did they send candidates which, on paper, matched our requirements, but also ones who through talking to them they felt would be an asset to our team. In fact, it was one of these candidates, who we may not have considered just from their CV, that we offered a position to.” - Cephalon

Job of the week - Senior Contract Regulatory Professional

Our client is a leading Pharmaceutical company. This R&D group have a large and dynamic European Regulatory Affairs Department responsible for the regulatory affairs work for the CNS R&D in Europe, Turkey, CEE region, Israel, South Africa, New Zealand and Australia.

The work has several aspects;

  • Communication to the Global Regulatory Teams and the supporting functions for regulatory submissions, such as clinical;
  • Working with the local operating companies within the^allocated region and external communication to regulatory authorities in the regions and to the EMEA. The group covers both developmental compounds not yet licensed and the maintenance and further development of marketed products. The prime responsibility for compounds is with the European Regulatory Liaison (EURL) who is responsible for the regulatory activities in the region and inputs to the global regulatory aspects for the compound.Regulatory consultants will work for an EURL or a global regulatory leader in the CNS therapeutic area or in the mature products area. They will work on the practical aspects of the compounds assigned from clinical trial applications (CTA’s), ASR’s, requests for scientific advice, MAA preparation, variations, renewals, PSURs etc depending on the life cycle of the compounds assigned. They may work on one or several compounds depending upon the work required for any compound at the time. Their work will be assigned and monitored by the EURL or theglobal regulatory lead responsible for the consultant.Eligibility to work in the EEA is required