IndustryAppointments.com

Main Tasks:

Knowledge Management
Review CS (concept sheet) and relevant documentation in advance of the CSRC (Concept Sheet Review Committee) meeting and prepare comments
Support the trial and project team with follow up of action, post CSRC meeting, and ensure that the final protocol is developed in compliance with the approved CS
Collect, compile, analyze and summarize the feedback received from the Ethics Committees and health authorities post submission of final protocols
To provide quarterly activity reports on the CSRC
Clinical trial results: review results in light of the history of the trial design development, from concept sheet to final protocol. Provide lessons learned as appropriate and keep up to date with new trial methodologies and methods

Medical Governance
Global Safety and Ethics Committee: review documentation provided in support to first-in-man and first in pediatrics, or other documentation prior to GSEC Global Safety and Ethics Committee) meeting and to support the trial and project team with follow up of action, post GSEC meeting
Support the Chief Medical Officer in other medical activities

Business Development
Coordinate the feedback on all in licensing opportunities across all Development functions


Skills and Qualifications:

Medical doctor with sound experience in drug development within the pharmaceutical or biotech industry
Clinical experience gained across various therapeutic areas, deep understanding of clinical trial designs and statistical concepts
Ability to analyze, interpret, present and publish clinical study results
Commitment to ethics and scientific standards
International experience
Open-minded and flexible in approach, convincing and effective communicator, oriented towards efficiency and results driven, team player
Fluent in English, our business language








Key information at a glance:

Start: asap
Location: Switzerland, Geneva
Industry: Pharmaceutical
Contract Type: Permanent
Referance No. 79702/11