About this opportunity
Hydrogen Group lists this Executive Director, Global Medical Affairs opportunity in trenton, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Executive Director, Global Medical Affairs
Executive Director, Global Medical Affairs
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.
Qualifications:
MD, PhD, or PharmD 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
Employment type
Full-time
Job function
Job function
Research and Science
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Worksite address
trenton, NJ, 08628, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.