Job Description

Role Summary:

• The US Regional Director Medical Affairs (RDMA), Prostate Cancer is responsible for driving the planning and execution of scientific & medical affairs plans in the Value & Implementation organization for the assigned therapeutic area (Prostate Cancer) in the United States, including Alliances with external partners as applicable. They are impactful members of regional cross-functional teams, including US Medical Affairs, Outcomes Research, Commercial, Clinical Operations, Policy and Market Access. They engage with their network of scientific leaders and decision makers in their region. This is a US-based position in Our Company's Research Laboratories, Global Medical and Scientific Affairs (GMSA).

Responsibilities and Primary Activities:

• Guides country Research Division GMSA staff to execute the annual scientific & medical plan for their assigned TA (Prostate Cancer), including Alliances with external partners as applicable.

• Co-chairs the US Medical Affairs Team (USMAT) to ensure development and execution of agreed medical affairs strategy and tactics to achieve the Value & Implementation (V&I) goals and priorities while providing strategic input at the global level

• Ensures scientific exchange is aligned with the global scientific and medical affairs goals and priorities

• Consolidates actionable medical insights from countries in their region

• Partners with regional Commercial, regional Outcomes Research, regional Policy and regional Market Access to drive development and execution of regional plans

• Engages with a network of scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) from their region about Our Company's emerging science

• Supports, as regional TA expert, affiliates staff in engagement with their national scientific leaders

• Organizes regional expert input events (advisory boards and group input meetings) to answer Our Company's questions about how to develop and implement new medicines or vaccines

• Organizes regional symposia and educational meetings as appropriate

• Reviews investigator-initiated study (IIS) proposals per established process

• Manages regional programs (patient support, educational or risk management) to support appropriate and safe utilization of our company's medicines

Required Qualifications, Skills & Experience:

Minimum:

• M.D., Ph.D. or Pharm.D.

• At least 3 years' experience in medical affairs in the US

• Minimum of 5 years Oncology experience

• Strong prioritization and decision-making skills

• Ability to effectively collaborate with partners across divisions in a matrix environment

• Excellent interpersonal, analytical, communication skills (written and oral) in addition to results-oriented project management skills

Preferred:

• Prostate Cancer role experience (3+ years)

• Customer expertise, especially of scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area

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.

We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. 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 diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

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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 Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education.

Expected US salary range:

Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.

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:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

*A job posting is effective until 11:59:59PM on the day BEFOREthe 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:R332461