Senior Manager, Medical Affairs Professional

Boston - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

This is a 1099 contract opportunity with no benefits.

This is a remote opportunity with occasional travel.

Key Responsibilities
Strategic Leadership

Develop and implement a comprehensive medical affairs strategy for marketed products and pipeline programs.
Serve as a key medical advisor to senior management and internal cross-functional teams.
Align medical plans with corporate goals regulatory requirements and evolving market needs.

Scientific and Clinical Expertise

Provide authoritative medical guidance for product development launch and lifecycle management.
Oversee preparation and dissemination of scientific data through publications presentations and educational materials.
Guide clinical trial strategy investigator-initiated studies post-marketing research and real-world evidence initiatives.

Stakeholder Engagement

Build and maintain strong relationships with Key Opinion Leaders (KOLs) investigators regulatory authorities and professional societies.
Represent the company at scientific congresses advisory boards and key external meetings.
Provide medical support for business development activities including due diligence and partnership evaluations.

Compliance and Governance

Ensure all medical activities comply with company policies FDA EMA ICH and other relevant regulations.
Oversee the review and approval of promotional materials medical content and external communications for scientific accuracy and regulatory adherence.

Qualifications

Advanced scientific or medical degree (MD PharmD or PhD) required.
5 to 10 years of progressive experience in medical affairs clinical development or related functions within the pharmaceutical biotechnology or medical device industry.
Demonstrated ability to design and execute medical strategies including product launches and lifecycle management.
Strong understanding of clinical research regulatory frameworks and medical communications.
Excellent leadership collaboration and communication skills with experience presenting to executive leadership and external stakeholders.

Important Notice: Protecting Your Information
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Required Experience:

Senior IC

This is a 1099 contract opportunity with no benefits.This is a remote opportunity with occasional travel.Key ResponsibilitiesStrategic LeadershipDevelop and implement a comprehensive medical affairs strategy for marketed products and pipeline programs.Serve as a key medical advisor to senior managem...

This is a 1099 contract opportunity with no benefits.

This is a remote opportunity with occasional travel.

Key Responsibilities
Strategic Leadership

Develop and implement a comprehensive medical affairs strategy for marketed products and pipeline programs.
Serve as a key medical advisor to senior management and internal cross-functional teams.
Align medical plans with corporate goals regulatory requirements and evolving market needs.

Scientific and Clinical Expertise

Provide authoritative medical guidance for product development launch and lifecycle management.
Oversee preparation and dissemination of scientific data through publications presentations and educational materials.
Guide clinical trial strategy investigator-initiated studies post-marketing research and real-world evidence initiatives.

Stakeholder Engagement

Build and maintain strong relationships with Key Opinion Leaders (KOLs) investigators regulatory authorities and professional societies.
Represent the company at scientific congresses advisory boards and key external meetings.
Provide medical support for business development activities including due diligence and partnership evaluations.

Compliance and Governance

Ensure all medical activities comply with company policies FDA EMA ICH and other relevant regulations.
Oversee the review and approval of promotional materials medical content and external communications for scientific accuracy and regulatory adherence.

Qualifications

Advanced scientific or medical degree (MD PharmD or PhD) required.
5 to 10 years of progressive experience in medical affairs clinical development or related functions within the pharmaceutical biotechnology or medical device industry.
Demonstrated ability to design and execute medical strategies including product launches and lifecycle management.
Strong understanding of clinical research regulatory frameworks and medical communications.
Excellent leadership collaboration and communication skills with experience presenting to executive leadership and external stakeholders.