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Vacancy details
Vacancy description:
Job Code:
Medical Director - Fr,Ger, Hun
Job Title:
Medical Director
Job Category:
CRM (Clinical Research Management)
Contract:
Permanent
Discipline:
Any Discipline
Country:
France, Germany, Hungary
Location:
Any Location
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
24 Jun 2008
Medical Director
Qualifications: Training & experience
A medical doctor (MD) board certified in internal medicine and with at least two to three years clinical experience in cardiology or oncology.
Full registration as physician and basic clinical research experience preferred.
Good communication and influencing skills required.
Ability to work in a team, with sensitivity and diplomacy.
Excellent English language skill. Other languages would be a plus.
Able to write clearly and present ideas in a logical fashion.
Board certification or eligibility in cardiology or oncology would be an asset.
Responsibilities:
The Medical Director manages and takes responsibility for medical and scientific aspects of phase I-IV projects in his therapeutic area in OCR International and/or globally, in collaboration with a matrix-structured team of professionals including clinical operations, proposals, business and project management. The primary objectives are:
To undertake feasibility work and formal feasibility studies, primarily in his therapeutic area (cardiology or oncology) but also in other therapeutic areas, as needed.
To collaborate with Business Development in the preparation of proposals as well as attend Bid defense meetings when required.
Approximately 15% travel is required.
To assist in the preparation of clinical development plans in collaboration with Clinical Writers.
To liaise with expert opinion in relevant therapeutic areas (primarily cardiology or oncology).
To organise expert meetings where appropriate.
To conduct a medical review of patients’ safety and laboratory data.
To communicate with investigators and site personnel as needed as a medical monitor.
To review clinical documentation (Protocol, Case Report Forms, Informed Consent, etc.) as required by Medical Writers.
To review Serious Adverse Event Reports as required by the Safety Department.
To be included in the rota for 24/7 coverage for Serious Adverse Event alerts (contactable via mobile phone).
International travel as required (investigator meetings, client interfaces, etc.)
Department: Medical/Safety
Location: Gentilly France, Eschborn, Germany, Budapest Hungary
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