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Executive Director, Global Medical Affairs
Job in
Trenton, Mercer County, New Jersey, 08628, USA
Listed on 2026-02-07
Listing for:
Hydrogen Group
Full Time
position Listed on 2026-02-07
Job specializations:
-
Healthcare
Healthcare Management -
Management
Healthcare Management
Job Description & How to Apply Below
3 days ago Be among the first 25 applicants
- Lead and manage the Global Medical Affairs team, ensuring alignment with corporate goals.
- Lead Advisory Board meetings according to the Global Medical Plan (GMP).
- Develop and implement Global Medical Affairs strategies to support the company's product portfolio.
- Lead the Global Medical Affairs Plan creation in collaboration with the cross-functional team.
- Collaborate with cross-functional teams, including R&D, Regulatory Affairs, Market Access, Marketing, and Commercial teams, to ensure cohesive and effective communication strategies.
- Oversee the development and dissemination of scientific and medical information to healthcare professionals, regulatory authorities, payors, and other stakeholders.
- Provide medical and scientific expertise to support clinical development, regulatory submissions, and post-marketing activities.
- Monitor and analyze industry trends, competitive landscape, and emerging scientific data to inform strategic decisions.
- Establish and maintain relationships with key opinion leaders, healthcare professionals, and industry organizations.
- Represent the company at scientific conferences, meetings, and other external events.
- Ensure compliance with all relevant regulations and guidelines, including GCP, and other industry standards.
- Manage Medical Affairs budget in alignment with forecast.
Job Description :
- Lead and manage the Global Medical Affairs team, ensuring alignment with corporate goals.
- Lead Advisory Board meetings according to the Global Medical Plan (GMP).
- Develop and implement Global Medical Affairs strategies to support the company's product portfolio.
- Lead the Global Medical Affairs Plan creation in collaboration with the cross-functional team.
- Collaborate with cross-functional teams, including R&D, Regulatory Affairs, Market Access, Marketing, and Commercial teams, to ensure cohesive and effective communication strategies.
- Oversee the development and dissemination of scientific and medical information to healthcare professionals, regulatory authorities, payors, and other stakeholders.
- Provide medical and scientific expertise to support clinical development, regulatory submissions, and post-marketing activities.
- Monitor and analyze industry trends, competitive landscape, and emerging scientific data to inform strategic decisions.
- Establish and maintain relationships with key opinion leaders, healthcare professionals, and industry organizations.
- Represent the company at scientific conferences, meetings, and other external events.
- Ensure compliance with all relevant regulations and guidelines, including GCP, and other industry standards.
- Manage Medical Affairs budget in alignment with forecast.
- MD, PhD, or Pharm
D with a strong background in Medical Affairs, and Clinical Development. - Over 5 years Medical Affairs experience within Oncology with at least 10 years of industry experience.
- Developing and implementing successful Medical Affairs strategies.
- Excellent communication, leadership, and interpersonal skills.
- Strong knowledge of regulatory requirements.
***************** Must have Oncology experience******************
*
...
Seniority level- Seniority level Executive
- Employment type
Full-time
- Job function
Research and Science
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