This is a full-time position, with a direct reporting to the Chief Medical Officer.
This position provides strategic leadership and tactical oversight for the clinical/medical aspects of all phases of the clinical drug development process.
This person is responsible for the design, development and execution of Clinical Development Plans (CDPs), clinical trials and protocols in accordance with applicable GCP regulations.
This person leads and contributes to the analysis of study results, the assessment of the extent to which the study(ies) has achieved clinical/regulatory objectives and the documentation of study results.
MD degree, a minimum of 10 years of clinical drug development experience (early phases and Translational Medicine preferred) in biotech or pharmaceutical industries
Strong knowledge of the pharmaceutical/biotechnology business, global drug development and regulatory processes
Excellent leadership abilities
Fluent in written and oral English
Ability to travel
If this sound interesting to you or someone in your network has the relevant skills please apply now or contact me with your CV:
Joana.hembach@epmscientific.com Phone +49 30 166 370 338
