Clinical Project Physician

30 Oct 2018
14 Feb 2019

Clinical Project Physician
Location: Switzerland
Position type: Permanent
Salary: Highly competitive

My client is an innovative biopharmaceutical company with its headquarters located in Switzerland, a European biotech hub. They specialise in the discovery and development of small molecules to treat and transform the therapeutic outcome of a number of diseases. Due to an expansion in their product portfolio they are seeking an experienced Clinical Project Physician to join their team.

Key Duties:
The overall duty of the Clinical Project Physician is to provide guidance, oversight and overall medical leadership on clinical development projects throughout the entire process of concept generation to design, implementation, execution and finally, submission/approval.

This can be broken down to the following key attributes:
Provide medical leadership for all responsible project activities this requires of comprehensive and deep understanding of the science, medicine, product environment and competition relating to the particular disease area.
Deliver all medical aspects of the Clinical Project Development Plan related to the indication and oversight of its implementation.
Contribute to the strategic decisions of the Life Cycle Team using medical and scientific input where appropriate.
Use knowledge and strategic expertise to provide an overall global strategy.
Medically support all assigned projects and be able to prioritise to ensure timely and on target delivery on set objectives in line with clinical development roles.
Provide medical input to the project related communication/publication plan.
Provide scientific and medical leadership externally.
Liaise, lead and provide expert consultation on aspects of clinical advisory boards and study specific committees.
Provide expertise on behalf of the company at key regulatory interfaces, investigator meetings and partner meetings.

Candidate requirements:
Solid clinical research within a pharmaceutical company or clinical research organisation (CRO).
Be MD qualified.
Experience in the oversight of clinical projects.
Experience in neurology, hypotension, insomnia is preferred.
Drug development experience.
Sound understanding of the regulatory requirements/ICH guidelines.
Excellent organisation, problem solving, interpersonal and communication skills.
Able to effectively negotiate with key stakeholders to influence and obtain their buy in agreement.
Excellent communication both written and spoken in English.

If you feel that this is the role for you then please email your CV to or alternatively, call me on 0049 711 222 54403.

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