Medical Director - Jakarta, Indonesia - Merck KGaA Darmstadt Germany

Merck KGaA Darmstadt Germany

Perusahaan Terverifikasi

Jakarta, Indonesia

1 minggu yang lalu

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Siti Nur

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Deskripsi

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics.

Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility.

Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life.

Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

NAME OF POSITION TITLE:
Medical Director Indonesia

REPORT TO:
President Director PT Merck Indonesia

WORK LOCATION:
Jakarta, Indonesia

ROLE PROFILE

Roles responsible for ensuring organisation's compliance with pharmaceutical regulations and laws as well as providing expertise on drug safety and medical topics in Indonesia
Provides medical expert advice to ensure accuracy of data to support existing or new product promotion. Develops medical product information and stays informed on scientific trends and competition. Maintains relationships with target opinion leaders and trains local teams in medical topics.

SCOPE OF PEOPLE RESPONSIBILITY

Medical Management and Leadership:

Rightsize Local strategies and tactical plans to the affiliate's business realities
Manage ontime/onbudget execution of tactical plan, including phase 4 studies
Manage a broad portfolio of Medical Affairs tactics, across therapeutic areas for assets at various stages of the lifecycle (ie phase 4 studies, med ed, field medical etc)
Lead efforts resulting in increased operating resourcing efficiencies in the affiliate by leveraging enterprisewide resources
Consolidate and share healthcare landscape (payor, patient, access) insights and translate those insights into affiliate strategies
Responsible for assigning, tracking and monitoring relevant KPIs and metrics for Medical affairs Department
Lead affiliate Medical Affairs yearly budget and business planning, prioritization and tradeoffs
Coleading Local TA, Launch and Brand Strategies and lead the Medical Affairs Tactics

Talent Management and People Development:

Lead talent review process and demonstrate follow through on Development Plans for Key Talent
Develop or improve area and or affiliate onboarding and training
Create action plan to ensure healthy succession pools for leadership position
Manage talent across variety of cultures, languages and backgrounds
Manage employees with a variety of performance records and capabilities
Serve as a role model and mentor not just within the function

Regulatory & Compliance Management:

Successfully collaborate and lead resolution of regulatory, reputational, compliance and other risk issues in the affiliate
Contribute to affiliate labeling discussions
Lead the problem solving process for significant safety or quality issues at affiliate
Deliver on postmarketing commitments on time and with quality
Manage ethical issues at affiliate to resolutions that satisfy business and societal needs
Participate in and contribute significantly to internal policy and external trade or regulatory working teams on matters that impact the affiliate

Scientific and Technical Leadership:

Meaningfully contribute to strategic and tactical discussions in crossfunctional leadership teams
Actively inform and contribute to GMA/RMA and local strategy and tactics in collaboration with Global/Regional TA's, GME and General manager
Collaborate with pharmacovigilance and regulatory in interpreting regulatory and safety risks in their geography
Manage effective scientific communication throughout their geography
Provide counsel on clinical and health outcomes research design and ensure that Country research proposals are scientifically and strategically aligned to global data generation priorities (Country Council)
Organize and Chair the Country R&D Council
May lead presentation and discussion on local Studies at internal study review committee meetings
Chair of the Local Quality and Safety Team (LQST)
Collaborate with Global/Regional TAs and RCO to ensure research activities are completed and published on time and on budget

EDUCATION

University degree (Bachelor's) required, preferably in scientific field of relevance to position
Secondary / advanced scientific degree (e.g., PharmD, PhD, DO, MD, MBBS) required
Other advan