- Build relationships with scientific thought leaders in one or more indications and therapeutic areas.
- Plan and organize advisory boards or other scientific meetings/symposia including preparation of agenda, material for speakers and own scientific presentations
- Provide medical support to marketing projects (Ad boards, webinars, symposia ...).
- Provide medical content for medical education programs and conduct formal presentations and clinical sessions upon request to external stakeholders.
- Build internal training programs to promote medical and scientific understanding of the products and perform internal trainings dedicated to sales reps and other affiliate employees.
- Attend regional, national and international medical conferences on the respective disease areas and provide reports from these meetings for internal stakeholders.
- Manage medical enquiries by internal and external customers including physicians and researchers, patient advocacy groups, and other key stakeholders (i.e. payors, health authorities at national or regional level, etc.).
- Support cross-functional colleagues with clinical data presentations, scientific intelligence, literature summaries, company trial site identification and be involved in clinically or scientifically-related initiatives/projects of interest to Grifols.
- Collect medical/scientific information from different sources including field-based insights and communicate to the appropriate internal functions and departments.
- Be responsible for the accuracy of the medical content of marketing materials and medical function in the sign off process of marketing materials.
- Be responsible for the knowledge management in your respective area including keeping up-to date with the current literature, updates, slide sets etc.
- Select and write summaries of relevant literature to support internal stakeholders.
- Contribute to scientific publications derived from Grifols projects or studies (including abstract writing or revision of manuscripts).
- Provide medical input in the development of Standard Operation Procedures (SOP) and value dossiers or other materials requested for regulatory purpose and market access support.
- Manage at a country-level Grifols Research programs, including ISR, RWE, Research Grants, Scientific Awards, and educational grants.
- You have a degree in Biology, Biomedicine, Biochemistry, Biotechnology, Pharmacy or Medicine. It will be an added value if you have a PhD, MD or PharmD with advanced knowledge in the respective scientific field.
- You have At least 4 years of experience in a Medical Affairs position in the pharma industry.
- You have expert knowledge of medical/pharmaceutical basics with highest ethical standards and scientific understanding (literature, clinical and basic research etc.).
- You have strategic thinking & influence and advanced communication and relationship building skills.
- You speak advanced level of French and English.
- You have willingness to travel.
- We are flexible with your location as you'll be covering the whole country.
- Benefits Package.
- Contract of Employment: Permanent position.
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Medical Affairs Manager France - Grifols, S.A
Description
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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
We are looking for a Medical Affairs Manager for France who will build and maintain relationships with scientific thought leaders and communicate relevant information from and to this group in close cooperation with local and global marketing groups among other departments. The products you will be working with are plasma derivative products used in various therapeutic areas (Pulmonology, Intensive care, Transplantation, Infectious Diseases ...).
What your main responsibilities will be
You will have the opportunity to:
Who you are
The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
What we offer
This is a a brilliant opportunity for someone with the right talents.
Information about Grifols is available at If you're interested in joining our company and you have what it takes, then don't hesitate to apply.
We look forward to receiving your application.
Grifols is an equal opportunity employer.
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Location: EMEA : France : Paris : Suresnes
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