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Head of Clinical Affairs

Пловдив България

You are the right fit for this role if you have:

  • experience in Clinical Affairs (managerial position experience is advantage);
  • training and detailed know-how of ISO 14155 and GCP;
  • at least 3 years in the area of Clinical trials (project management, monitoring, etc.);
  • fluent English (speaking and writing skills);
  • strong verbal, written, interpersonal communication skills;
  • enthusiastic, willing to improve and develop the clinical trial related activities and processes;
  • medical or pharmaceutical education is considered an advantage;
  • experience with medical device regulatory requirements is considered an advantage.

As Head of Clinical Affairs you will be responsible for:

  • management of growing Clinical Affairs team;
  • project management of the Medical Device Studies intended for regulatory purposes;
  • often communication with Regulatory Affairs and R&D center in Prague;
  • participation in study design, writing, evaluation, monitoring etc.;
  • searching for new possibilities of doing clinical studies outside Bulgaria.

*The interview will happen in English language with representatives from Headquarters in Prague, Czech Republic.

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