Global Medical Manager
Vor 3 Tagen
**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.**
**Global Medical Manager M/F/d**
**YOUR TASKS AND RESPONSIBILITIES**
Medical Affairs generates evidence and translates the science of our brands to support the company’s overall purpose of empowering the transformation of everyday health.
The Global Medical Manager is a member of the Regulatory / Medical / Safety / Compliance (RMSC) team who leads medical activities working with R&D and Global Category Business Unit (GCBU) functions and driving business growth through innovation and business protection projects.
**THE FOLLOWING RESPONSIBILITIES ARE AWAITING YOU**:
- Maintaining the ability to translate scientific knowledge to support commercialization activities such as advertising claims substantiation and defense and new product opportunities for the TA category;
- Utilizing strategic planning, guidance and implementation of medical programs, such as pre
- and clinical studies;
- Supporting the development and is responsible for communication and execution of medical strategy regarding business opportunities and decisions where there is medical or clinical context;
- Representing medical governance for the TA (e.g. Approve advertising copy and promotional copy);
- Contributing to the development of strategy for thought leader identification, management and engagement in line with the therapeutic area strategic objectives and in compliance with legislation and Bayer Consumer Health rules;
- Contributing to regulatory activities (e.g. label maintenance and improvement, creating clinical sections of regulatory filings);
- Liaising with PV, Regulatory Affairs, Compliance (RMSC) and GCBU and relevant countries representatives in all projects to ensure the full assessment of needs and deliverables to positively impact and drive business with commercial functions.
**WHO YOU ARE**
- Healthcare professional (PharmD, PhD or MD) with 2 years of postgraduate training or equivalent experience within the pharmaceutical industry, preferable experience in mental health
- Experience in medical affairs, and/or clinical research and development;
- Sustain having a good understanding of the preclinical and clinical trial design elements, including statistical considerations, operations and interpretation of these activities as well as regulatory requirements for consumer health products;
- Demonstrates knowledge of scientific information searches, key opinion leader development and clinical knowledge;
- Displays excellent interpersonal communication and presentation skills, including the ability to network and manage stakeholders. Pro-activeness and result driven as well as highly customer oriented.
LI-CH
**YOUR APPLICATION**
**Location**:
Switzerland : Basel-City : Basel
**Division**:
Consumer Health
**Reference Code**:
782374
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