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 Affairs Physician Reproductive Health (all genders) 

 

YOUR TASKS AND RESPONSIBILITIES

 

Bayer is a recognized leader in Women’s Healthcare, with a strong footprint in contraception, gynaecological therapies, and menopause management. An exciting new role has been created to support the existing Reproductive Health portfolio with focus on lifecycle management. You will work in a cross functional Team, with Global colleagues from different areas (Commercial, Regulatory, Safety, Development and Communications) and medical affairs colleagues from countries and regions as well external stakeholders. We are looking for creative personalities with strong autonomy and project management skills who are energized by working in small agile teams. This role offers the opportunity to develop a set of broad skills and work in a multidisciplinary environment within a team that is passionate about Women’s Healthcare.

The primary purpose of this role is to provide medical input and scientific guidance to implement programs and scientific communication related to Bayer´s Reproductive Health franchise. The position holder will be responsible for supporting the Product Team providing medical input in projects with different stakeholders (Commercial, Regulatory, Safety, Clinical Development, External Scientific Community, Local Medical Affairs teams).

 

Key Tasks:

Provides medical input and supports the execution of the Medical Affairs Plan for the Reproductive Health franchise in alignment with the Product Team and key stakeholders. Plans and Executes Scientific Congress activitiesConceptualization and Review of high-quality educational materials Support Scientific Publications Close collaboration with the Commercial team to support business needs by providing medical background. Provide input on global promotional materials, ensuring scientific accuracy and compliance with SOPs and support development of materials for internal training and medical information. Provide Medical Affairs input into core labeling, pharmacovigilance documents and key "license-to-operate" topics for the Reproductive Health portfolio. Establish and manage compliant and sustainable scientific relationships with relevant stakeholders, supporting planning and conduct of scientific and educational events. Support organization of MA led studies in collaboration with cross functional groups; review Investigator Initiated Research projects in accordance with the respective strategy and SOPs Analyse and interpret results of clinical studies, medical affairs studies, Investigator Initiated Research projects, real-world-evidence data analyses as well as guidelines, presenting results to internal and external stakeholders

 

WHO YOU ARE

 

Medical degree, or equivalent (MD, MPH or Global Health, PhD) with understanding of clinical judgement knowledgeExperience or special interest in gynaecology/reproductive health/contraception/women’s healthcare and family planning (highly preferred) Excellent ability to conduct systematic literature reviews and critical appraisal of scientific publications Understanding of the different Healthcare settings around the Globe and unmet needs in WHC At least 2 years of experience in industry or biotech equivalent in a global or regional/country level or academic setting Good understanding of Pharma Compliance regulations in handling of external communication Strong project management skills: able to prioritize multiple tasks and goals and aim towards timely, on-target and within-budget execution High attention to detail and proven ability to drive results at a higher level of quality as a strategic and creative thinker, with open and supportive mindset Effective communicator with good presentation and writing skills Ability to act effectively and successfully in a complex global and multicultural environment and demonstrate sensitivity for cross-cultural differences Works well within teams, with experience in working across boundaries and building effective working relationships Strong ethical standards, compliant with global regulations, company policies and processes Ability to support designing, interpreting and communicating clinical studies/data and present complex information in different formats, appropriate to the specific audience Knowledge of the drug development process over different stages Understanding of general business concepts and the needs to achieve results in a challenging environment Fluent in English, both orally and in writing

 

We are looking forward to receiving your application by 30th January. Thank you!

  YOUR APPLICATION   

Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

Bayer is committed to providing barrier-free access and support-facilities for individuals with disabilities - during the application process and beyond. Applicants with disabilities are encouraged to request any support / equipment they may need via the contact information below.
 

 

 

Location:

Switzerland : Basel-City : Basel  

 

Division:

Pharmaceuticals

 

Reference Code:

837644