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Global Medical Director / Global Scientific Director (m/f/d)

Eingestellt von Hays aus Mannheim, Universitätsstadt

Gesuchte Skills: Engineering, Affiliate

Projektbeschreibung

REFERENCE NUMBER:

490918/1

MY DUTIES:

- Evidence Generation Strategy Planning and Execution
- Accountable for evidence generation activities for the assigned product (s) / Indication(s), including risk benefit assessment and medical monitoring in all medical affairs interventional studies
- Takes the role of Lead Scientific Responsible and acts as a member of the Study Management Team (SMT)
- Conduct review and approval of investigator initiated studies (IIS) and supported study proposals (incl. Review of affiliate study synopses and sign off of affiliate studies)
- As appropriate, provides medical expertise and scientific data to support Regulatory, Drug Safety, Health Economics and Public Policy strategy and documents
- As appropriate, represents PDMA and provides medical expertise to the appropriate Global Access teams and other relevant teams
- For some projects, the GMD may drive and lead the strategy of the integrated evidence generation activities, incl. Roche sponsored clinical studies, Investigator Initiated Studies (IIS), RWD
- Develop, advances and maintains TAE interactions and collaborations, incl. those aimed to set up and conduct evidence generation activities
- Represents Roche in peer-to-peer interactions with external collaboration partners, including in patient-company interactions. 
- Responsible for acting in line with legal, regulatory and company standards and codes of Practice
- Complete all required training modules as priority

MY QUALIFICATIONS:

- Profound experience in pharma (either in Medical Affairs or Clinical Operations) 
- Experience in clinical study set up and management on a global level 
- Scientific education minimum Master or PhD
- Experience in Oncology / GI Cancer (GI Cancer is a plus but not at all necessary) 
- Experience with China as part of a global clinical study 
- Clinical Research additional trainings 
- Experience of partnership with therapeutic area experts and external organizations is strongly preferred 
- Previous experience with launch of drugs/indications is preferred

MY BENEFITS:

- Dynamic and innovative market environment
- Flat hierarchies
- Good infrastructure
- High proven employee satisfaction based on annual surveys

ABOUT 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.

MY CONTACT AT HAYS:

My contact person
Marija Tomas

Reference number
490918/1

Contact
E-Mail: [email protected]

Projektdetails

  • Einsatzort:

    Basel Stadt, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    12 MM++

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Hays

  • Straße:

    Willy-Brandt-Platz 1-3

  • Ort:

    68161 Mannheim, Universitätsstadt, Deutschland