Medical Scientific Advisor (Temporary 9 Months) 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.
Purpose:
The Medical/Scientific Advisor acts as the primary scientific expert in the Therapeutic Area proactively providing training, scientific advice and strategic input to internal and external stakeholders as well as the scientific community.
The position holder shall drive the localization of the global medical and brand strategy in alignment with cross-functional, local and regional strategic partners. The incumbent is accountable for scientifically validating all materials and developing and contributing to multichannel campaigns and relevant scientific materials. The Medical/Scientific Advisor contributes to the generation of clinical evidence to address information gaps for the products across the life cycle.
Scope (global, regional or local):
Local
Key Tasks:
STRATEGIC CONTRIBUTION
Responsible and accountable for driving the localization of the global medical and brand strategy, by using local field insights and partnering with both local cross-functional teams and regional teams.
Responsible and accountable for using cross-functional knowledge to create medical multichannel campaigns: including content development, multichannel strategy and the customer journey.
Responsible and accountable for driving a strategic partnership with local cross-functional teams.
Accountable for aligning evidence generation with medical and brand strategy; including ensuring proper alignment for defining the scope of potential Observational Studies (OS) and Investigator Initiated Research (IIR).
DATA COLLECTION, ANALYSIS AND INTERPRETATION
Accountable for providing medical support to clinical trial teams on subjects related to interventional clinical trials including feasibility & initiation visits.
Accountable and responsible for managing study-related medical activities for Interventional Post-Approval Trials (IPAT), Observational Studies (OS) and Investigator Initiated Research (IIR) as locally required.
Responsible and accountable for reviewing and interpreting analytics and relevant field insights to optimise and manage medical content and adapt the evidence generation plan (e.g. in National Advisory boards).
MANAGING EXTERNAL RELATIONSHIPS
Responsible and accountable for fostering Medical Affairs relationships with Thought Leaders and external stakeholder groups e.g. healthcare organisations, medical societies, research groups, patient groups, government/ regulatory institutions.
Responsible for reporting external stakeholder engagement activities in Veeva Medical CRM.
MEDICAL EDUCATIONAL PROGRAMMES
Accountable for providing scientific contributions to the development and implementation of Bayer organised national, regional and local medical educational programs (e.g. Continuing Medical Education programs).
INTERNAL SUPPORT
Responsible and accountable for providing medical support on internal projects e.g. pre-launch activities, reimbursement processes, dossier development, commercial campaigns etc.
Responsible for aligning with internal functions to review Summary of Product Characteristics responsibilities including translations and updates.
Responsible and accountable for proactively ensuring that Bayer medical activities are in-line with relevant guidelines, regulations and legislations.
Responsible for providing scientific education and training to cross-functional partners (e.g. Sales and Marketing) on product data, therapeutic area knowledge, and local clinical operations and clinical development studies.
Responsible and accountable for scientifically reviewing and approving all therapeutic area/product related materials, external communications and advising cross-functionally using medical/scientific expertise.
MEDICAL QUERIES
Responsible for documenting and processing medical Information queries in alignment with local Medical Information handling procedures.
Key Working Relation:
internal:
Country Medical Director (CMD); Therapeutic Area in Global Medical Affairs (GMA); Medical Affairs colleagues (Country Level); Marketing & Sales organization (local Business Unit);
Pharmacovigilance; CAO Platform Functions (Procurement, Finance Business Partner, Accounting, Legal, Human Resources); Medical Information; Clinical Development and Clinical Operations; Regulatory Affairs; Market Access external:
Thought Leaders and investigators in the respective Therapeutic Area; Ethic and Regulatory Authorities (Clinical activities; Registration); Professional Societies related to the respective Therapeutic Area.
Skills & Qualifications:
Strong scientific/ medical background. Qualified Physician / Pharmacist / Biologist / high level of natural science education.
Desirable previous experience of being a Medical/Scientific Advisor in industry
Strong skills in managing stakeholders and experienced in building networks.
Business Acumen displaying ability to operate cross-functionally, driving organizational growth, understanding of marketing/sales functions in pharma industry.
Desirable experience contributing to an organization's strategic endeavours, displaying industry/market knowledge.
YOUR APPLICATION
This is your opportunity to tackle the world's biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.
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.
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