Regional Medical Affairs Director

2 months ago

Singapore GMP TECHNOLOGIES (S) PTE LTD Full time
Roles & Responsibilities

GMP is partnering with a leading pharmaceutical company dedicated to advancing healthcare through innovative medicines and therapies to identify a Medical Affairs Director to help lead their Asia Pacific region . With a focus on patient-centricity and scientific excellence, our client strives to improve patient outcomes and enhance quality of life across diverse therapeutic areas.

We are currently seeking a highly qualified and experienced Medical Affairs Director to lead our Medical Affairs team and drive strategic initiatives to support our mission.

Position Overview: As the Medical Affairs Director, you will be responsible for providing strategic leadership and direction to the Medical Affairs department. You will play a pivotal role in shaping the medical strategy, fostering relationships with key opinion leaders (KOLs), and ensuring the scientific integrity of our products. The ideal candidate will possess a strong background in medical affairs, exceptional leadership skills, and a passion for driving innovation in healthcare.

Responsibilities:

  1. Strategic Leadership:
    • Develop and execute the medical affairs strategy in alignment with business objectives and regulatory requirements.
    • Provide leadership and guidance to the Medical Affairs team, fostering a culture of scientific excellence, collaboration, and continuous improvement.
    • Drive cross-functional collaboration with internal stakeholders, including Clinical Development, Regulatory Affairs, Commercial, and Market Access, to support product development and launch activities.
  2. KOL Engagement and Scientific Exchange:
    • Cultivate and maintain relationships with key opinion leaders (KOLs), academic institutions, professional societies, and other external stakeholders.
    • Lead scientific exchange initiatives, including advisory boards, symposia, and educational programs, to disseminate clinical and scientific information about our products.
    • Collaborate with Medical Science Liaisons (MSLs) to identify and engage with KOLs and other healthcare professionals to gather insights and support evidence-based medicine.
  3. Medical Strategy Development:
    • Drive the development and execution of medical plans, including publication plans, investigator-initiated research (IIR) proposals, and medical education initiatives.
    • Provide strategic input into clinical trial design, protocol development, and data analysis to generate robust clinical evidence and support product differentiation.
    • Monitor and analyze scientific and clinical developments within relevant therapeutic areas to inform medical strategy and decision-making.
  4. Compliance and Regulatory Affairs:
    • Ensure compliance with relevant regulations, guidelines, and ethical standards governing medical affairs activities.
    • Collaborate with Regulatory Affairs and Legal teams to review promotional and educational materials for scientific accuracy and compliance with regulatory requirements.
    • Provide scientific support for regulatory submissions, including clinical data review and interpretation.

Qualifications:

  • Advanced degree in Medicine, Pharmacy, or Life Sciences (MD, PhD, PharmD, or equivalent).
  • Minimum of 10 years of experience in medical affairs roles within the pharmaceutical industry, with a proven track record of leadership and strategic thinking.
  • Strong understanding of clinical research methodologies, regulatory requirements, and medical ethics.
  • Excellent communication and presentation skills, with the ability to effectively engage with internal and external stakeholders.
  • Demonstrated ability to lead and develop high-performing teams in a fast-paced and dynamic environment.
  • Proven ability to think strategically, analyze complex issues, and make data-driven decisions.
  • Flexibility to travel as needed for KOL engagement, scientific conferences, and other business activities.

To find out more about this opportunity, please contact Steffan Lian at Steffan.Lian@gmprecruit.com
We regret that only shortlisted candidates will be notified.

GMP Recruitment Services (S) Pte Ltd | EA Licence : 11C3793 | Lian Cher Chieh | Registration No: R 1217705


Tell employers what skills you have

Pharmaceutical Industry
Leadership
Clinical Research
Regulatory Affairs
Healthcare
Medicine
Market Access
Clinical Development
Medical Affairs
Protocol
Advisory Boards
Compliance
Advocacy
Presentation Skills
Evidence
Case Management
Life Sciences
Therapeutic Areas
Medical Education

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