Sr Medical Manager Digestive Health - Basel, Schweiz - Bayer

Bayer

Geprüftes Unternehmen

Basel, Schweiz

vor 1 Woche

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

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.

Sr Medical Manager Digestive Health M/F/d

YOUR TASKS AND RESPONSIBILITIES

Medical Affairs generates and translates the science of our brands to support the company's overall purpose of empowering the transformation of everyday health.

The Global Senior Medical Manager (GSMM) is a senior medical responsible for leading, developing and implementing the Medical Affairs, Evidence Generation and Scientific communication strategy for the Bayer Consumer Health (BCH) demand space within Digestive Health in partnership with other functions within Medical Affairs and Evidence Generation Team.

The GSMM is a key partner for R&D/Regulatory, Medical, Safety and Compliance (RMSC) and Global Category Business Unit (GCBU) functions in driving business growth through innovation and business protection.

Through a comprehensive understanding of substantial body of medical/scientific information and development of the assigned relevant therapeutic area and benefit spaces, as well as of the markets where BCH is present, unmet needs and regulatory landscape, the purpose of the GSMM position in Digestive Health is to develop and execute robust medical strategies in line with the category strategy to ground BCH products and developments in science, thus ensuring they can be recommended as first choice by HCPs and are the preferred option by consumers.

The GSMM defines and implements exploratory and clinical activities as well as medical strategy for the pre-NPD (New Product Development) and NPD portfolio in the assigned therapeutic area.

The GSMM provides contribution to all functional areas of RMSC, R&D and to the GCBU in Digestive Health from scientific/medical/clinical perspective.

S/he can be delegated to support implementation of BHC Medical and Regulatory Governance framework within the BCH division. S/he is a key liaison with PV, Regulatory Affairs, GCBU and relevant countries representatives. For the assigned brands, the incumbent leads the Medical Brand Team meetings with the key countries. S/he is accountable for the overall quality and compliance for TA Medical Scientific Writing.

Main tasks:

Proactively seeks in the assigned area of responsibility for development and maintenance of comprehensive understanding of the current and emerging science/medical insights and needs, state of the art clinical trials methodologies/endpoints in Digestive Health, including respective treatment, prevention, and other selfcare measures.
In alignment with the Digestive Health category strategy develops and implements medical plans/strategy to maximize brand and portfolio innovation and business opportunities, including, but not limited to, new products, indications, claims, and communication.
Defines and coordinates relevant medical/scientific activities for new product developments as well as product maintenance/life cycle management (clinical studies, publications, scientific congresses, Investigator Initiated Research IIRs) in the Digestive Health category in alignment with the category strategy.
Engages and supports the development of the strategy for key opinion leader management in line with Digestive Health strategic objectives and in compliance with legislation and BCH rules, e.g. advisory boards, scientific symposia, webinars.
Assumes leadership for medical input to core labelling and pharmacovigilance documents (e.g. global source texts, company core data sheets, risk management plans, period benefit risk evaluation reports).
Coordinates the preparation of medical documents for submission to regulatory authorities in the assigned portfolio, incl. updates of existing dossiers for OTC products, Medical Devices, cosmetic products.
Ensures customer centric approach in line with identified medical needs throughout all initiatives, embraces the 4 company's focus behaviors Experimentation, Collaboration, Customer Focus and Trust and builds appropriate relationships internally and externally.

WHO YOU ARE

PhD, MD, PharmD in natural sciences, Pharmacy, Biology, Medicine, Chemistry
Minimum of 5 years' experience in consumer healthcare or pharmaceutical organization, in a local or global scientific/medical function
Experience in Digestive Health is an asset
Strong and flexible team player
Experience of participating in crossfunctional teams across different cultures and geographies
Experience