US Regional Director Medical Affairs (RDMA) – CMV/Antifungals

Date: Jan 11, 2019

Location: Upper Gwynedd, PA, US

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Requisition ID: MED004048

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.


Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 

 

The US Regional Director Medical Affairs (RDMA) – CMV/Antifungals is responsible for driving execution of scientific & medical affairs plans for their assigned Therapy Areas (TA) in the U.S. They are an impactful member of regional cross-functional teams, including US Commercial, Center of Real-World Evidence (CORE), Policy and Market Access. This is a US-based position in Merck Research Laboratories Global Medical Affairs (MRL GMA) residing in PA or NJ.

 

Primary activities

  • Guides medical and scientific staff to execute the scientific-medical-research (SMART) plan for their assigned TA.
  • Co-chairs the US scientific-medical-research (SMART) team to ensure execution of agreed medical tactics and leverage best practices
  • Provides medical input to Product Development team (and sub-teams)
  • Partners with US Commercial, CORE, Policy, and Market Access to drive development and execution of US scientific-medical-research plans.
  • Ensures scientific exchange is aligned with the global scientific communications platform
  • Consolidates actionable medical insights from the US.
  • Engages with a network of scientific leaders and other key stakeholders (e.g., therapeutic guideline committees, payers, public groups, government officials, medical societies) from the US.
  • Supports, as US TA expert, engagement by US field scientific and medical leads within US Commercial Operations
  • Organizes and leads US expert input events to answer Merck’s questions regarding how to optimally implement new medicines (e.g., advisory boards and expert input forums)

 


Qualifications

Education:

Minimum Requirement:

MD, PharmD, or PhD and recognized medical expertise/specialization in Infectious Diseases and/or Transplant Medicine  

 

Required Skills:

• Experience in Medical and/or Scientific Affairs

• Strong prioritization and decision-making skills

• In a matrix environment, able to effectively collaborate with partners across divisions

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

 

Preferred

• Medical and/or scientific affairs experience

• Scientific leadership and skills in engaging other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area

• Recognized expertise through 5 years clinical and/or research experience (including publications) in therapy area   

 

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 

 

If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com.

  

Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 

          OFCCP EEO Supplement

 
Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations.


Job: Medical Affairs Generic
Other Locations: NJ, US
Employee Status: Regular
Travel: Yes, 25 % of the Time
Number of Openings: 1
Shift (if applicable): N/A
Hazardous Materials:
Company Trade Name: Merck

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