Study Responsible Physician (m/f/d)

Basel Land | Freie Mitarbeit 
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Kategorie(n): Gesundheit
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Projektbeschreibung

Referenznummer: 487398/1
Startdatum: asap
Projektdauer: 6 MM+
Ort: Basel Land

Meine Aufgaben:
  • Responsible for medical monitoring/reporting and company safety officer activities
  • Work on clinical development plans, trial protocols and takes ownership of clinical study reports
  • Evaluate adverse events (pre and post-marketing) for relationship to treatment 
  • Assist Regulatory Affairs in determining requirements for any corrective actions or health authority reporting
  • May act as a medical contact at the company for health authorities concerning clinical/medical issues
  • Interpret, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissions
  • Close interactions with Project Scientists and Physicians across programs
  • Assist Regulatory Affairs in the development of drug regulatory strategies
  • Help explore and evaluate new product ideas to assist in identifying new market opportunities
  • Support general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance
  • Participate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.
  • Review medical literature and related new technologies
  • May be asked to assess medical publications emerging from the Team and its affiliates
  • May be responsible, with appropriate colleagues, for review of Company advertising and promotional materials
Meine Qualifikationen:
  • MD (or equivalent) in neuroscience (neurology or psychiatry) with appropriate post-doctoral training and certification
  • Fluent in written and spoken English
  • Working knowledge of the use of Microsoft suite of software products including Excel and Word
  • Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings
  • Experience in late stage clinical development of disease modifying treatments for MS
  • Experience in clinical development of S1P receptor modulators highly preferred
Meine Vorteile:
  • A city with a high quality of life that perfectly embraces both modern and traditional values
  • A highly motivated team and an open way of communication
  • A very renowned company
Über Hays:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.


Einsatzort: Basel Land

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