VP, Global Medical & Scientific Affairs, General & Specialty Medicine TA

Job Description

The Vice President, Global Medical and Scientific Affairs (GMSA), Therapy Areas builds and develops teams accountable for Therapy Area (TA) leadership, strategic planning, and execution for therapy areas globally. Their teams cover all therapy areas in their portfolio. As member of the Company Research Laboratories Global Medical and Scientific Affairs (Research & Development (R&D) GMSA) Leadership Team they partner with other R&D GMSA leaders to maximize all medical and scientific activities are aligned with R&D GMSA's priorities and demonstrably address opportunities/challenges in countries and regions.

The Vice President (VP) partners with the Research Leadership Team, commercial Customer Business Lines/ Global Marketing and Country Leaders of US, Japan, China. The VP is a company ambassador for the scientific & medical community and key decision makers. They co-strategize with the Center of Real-World Evidence (CORE), Policy and Market Access management and can be a member of their extended leadership teams.----------

Primary Responsibilities:

• Builds, develops and leads teams of therapeutic area (TA) dedicated staff (Associate Vice President (AVP), Executive Directors, global and regional directors and associate directors)
• Ensures that the annual scientific & medical plans developed by their teams guide TA scientific exchange (input and output) of all R&D GMSA staff globally. Organizes approval of these plans by the Senior Vice President (SVP) R&D GMSA and Senior Vice President, Global Clinical Development
• Aligns budgets for staffing and R&D GMSA activities with the SVP R&D GMSA and manages these budgets appropriately
• Creates cross-functional Scientific Medical and Research Teams to realize scientific value creation through responsive scientific leader interactions, a unified scientific/medical understanding and viewpoint, and aligned scientific exchange execution
• Contributes to commercialization strategies and global clinical development plans, partnering with Global Clinical Development and Commercial management (global, US, regional, Japan and China)
• Contributes to the Center of Real-World Evidence (CORE) book of business with recommendations about CORE's portfolio and by leading local data generation that complements CORE's portfolio. Ensures that all local data generation activities follow appropriate CORE governance
• Is (or assigns AVP as) the Medical Head in alliances with partner companies
• Ensures the TA teams have a solid understanding of how countries' medical systems and standards of care have to change to accept new innovation, how to introduce the new innovation and how to implement and maintain its use
• Infuses company decisions (Clinical Development or Commercial) with actionable medical insights collected by the teams from countries and regions
• Is a company ambassador for US/EU Medical Professional Societies, global key stakeholder organizations
• Leads comprehensive stakeholder engagement plan about Our Company's emerging science, spanning global, regional and key country scientific leaders and key decision makers (therapeutic guideline committees, payers, public groups, government officials, medical societies) from phase 2b to end of life cycle
• Complements the stakeholder engagement plan with programs / expert input events to answer Our Company's scientific questions regarding how to develop and implement new medicines or vaccines: advisory boards and expert input forums
• Develops teams so that they provide relevant contributions as members of the Product Development sub-teams (Value Evidence, Clinical, Commercial, Publications and Label teams)
• Organizes regular management reviews of the teams' activities and progress
• Oversees the development and execution of global and regional symposia and educational meetings
• Supports the investigator-initiated study program
• Supports business development assessments by validating unmet medical needs, reviewing asset data and recommending required Medical Affairs resources
• Leads talent review process and demonstrate follow through on Development Plans for Key Talent
• Creates action plans to ensure healthy succession pools for leadership positions within the teams and in R&D GMSA

Education:

M.D. and recognized scientific expertise

Required Experience and Skills:

• Extensive experience in Medical Affairs or Clinical Development
• Demonstrated ability to chart the course and build successful teams
• Gravitas with Our Company's senior management (R&D and Human Health)
• Track record of contributing to company decisions in the broader context of its corporate strategies
• Able to effectively collaborate with and influence partners across divisions within a matrix environment
• Has managed resourcing, budgeting, and budget prioritization

Preferred Experience and Skills:

• 15 plus years global or US Medical Affairs or global clinical development experience with proven track record of successful medical or clinical development strategies
• Customer expertise especially scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations)

Required Skills:
Accountability, Accountability, Book Of Business, Business Development, Business Value Creation, Clinical Development, Clinical Research, Communication, Cross-Cultural Awareness, Emerging Technologies, Ethical Compliance, Healthcare Education, International Marketing, Key Opinion Leader Management, Leadership, Marketing, Medical Affairs, Medical Knowledge, Medical Marketing Strategy, Mentoring Staff, People Leadership, Pharmaceutical Medical Affairs, Professional Networking, Public Speaking, Research and Development {+ 5 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote".

The salary range for this role is
$378,100.00 - $595,100.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at .

You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.-

Employee Status:
Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:
Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:
06/6/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID: R388237