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Archiviertes Projekt - Medical Director

Juli 2019

CH-Lausanne

auf Anfrage

10.07.2019

124079_1562753108

Projektbeschreibung

We are recruiting for a Medical Director within CNS for our Biotech client in Switzerland.

You will bring exceptional leadership qualities to different clinical programs across various indications, involving multiple compounds. You are accountable for the strategy, design, implementation, and execution of a clinical development programs to support decision milestones, regulatory requirements and market access.

Responsibilities:

* Will represent Clinical Development and lead Global Development and Program Teams
* Will Lead teams to drive transition of pre-Proof of Concept to Development. You will lead the development and execution of the clinical strategy. You will develop plans designed for successful global regulatory approval and market access for multiple treatment indications.
* Leads the creation of key clinical documents: Clinical Trial Protocols (CTPs), Investigator's Brochures, Clinical Study Reports (CSRs), regulatory documents including maintenance of product licenses, registration dossiers, value dossiers, pharmacoeconomic dossiers.
* Supports registration, market access, commercialization, and maintenance of product licenses.
* Together with Patient Safety, ensures continuous evaluation of drug safety profile, including safety monitoring of clinical studies and signal detection from post-marketing surveillance.
* As the medical expert, leads interactions with external stakeholders: regulatory authorities, data monitoring committees, advisory boards, patient advocacy groups; internal stakeholders: Research, Translational Medicine, Global Medical Affairs (GMA), Marketing, Health Economics & Outcomes Research)
* Plans and executes publication and clinical communication strategy in coordination with GMA and Medical Writing, and provides input into key external presentations
* Drives scenario development for Clinical Development to support decision analysis and optimal resource allocation.
* Leads or serves as Subject Matter Expert for Clinical Development line function initiatives

Education:

* Medical Doctor within the specialised area of Neuroscience/Neurology; Medical Board certification preferred for MD

Experience:
· 10+ years of involvement in clinical research or drug development in an industry environment spanning clinical activities in Phases I through III/IV, including submission dossiers
· Advanced knowledge of CNS therapeutic area - and preferably within Multiple Sclerosis.
· Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory/clinical development process
· Experience with submissions and health authorities required
· Demonstrated ability to establish strong scientific partnership with key stakeholders
· Demonstrated leadership and management skills with a documented track record of delivering high quality projects, submissions, trials in a global and matrix environment (including remote) in pharmaceutical or biotech industry

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