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Merck & Co, Inc

US Scientific Director Medical Affairs - HIV ( MERCUSR108517ENUS)

Science and Research

Medical Illustrator

Yearly

No

North Wales, Pennsylvania, United States

Job Description

Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio.

The US-Scientific Director, Medical Affairs (SDMA) drives US/Global Strategic alignment and optimizes Field readiness across USMA’s five functional pillars (1. Scientific Exchange; 2. Company Trials; 3. Investigator Sponsored Programs 4. Congresses; 5. Insights). The SDMA is an experienced therapeutic area leader/ subject matter expert with experience in HIV/virology who possesses relevant medical affairs and field medical (FM) experience to guide and direct field medical strategy and anticipate regional FM needs in alignment with US/global medical affairs and organizational priorities. Along with the USMA Field Leaders (ED/AVP), the SDMA is responsible for regional Field Medical strategy and prioritization of Global Plans for US Medical Affair.

As co-lead of the US Regional Medical Affairs Team (RMAT), the SDMA partners with the Global TA team and cross-functional members to enable US regional implementation of the Global Strategic Medical and Research (SMART) Plan. This includes review, translation, summarization and pull through of US scientific leader (SL) field insights, facilitating local pull-through of global strategy and consulting on the development and execution of aligned local content and training needs. This is a regionally based position (US) in our Company's Research Laboratories, US Medical Affairs (MRL USMA).

Responsibilities and Primary Activities:

  • Partners with Global Scientific Training (GST), Global Scientific Content (GSC), US Global Clinical Trial Organization, (GCTO), GMSA TA leads, and relevant internal and external subject matter experts to consult and assist in the delivery of regional training needs, as needed.

  • Serves as a key scientific interface between GMSA and HQ functions and the US field.

  • Works closely as a member of the ID/V/V USMA LT and has responsibility for scientific aspects field strategy and execution, including the integrated US Country Medical Plan, including US Field Execution Plan (FEP) and field training plan for assigned therapeutic area.

  • Collects and communicates scientific insights from US field engagements to inform company strategies, as per the GMSA (therapeutic area) TA needs

  • Actively participates in bi-directional information exchange and sharing of best practices across the various roles and teams in USMA, including Health Systems, to optimize USMA Field execution

  • Collaborates to prioritize Regional Medical Science Director (RMSD) activities to advance our Company's research studies, company-sponsored trials, and others) in collaborations with GCSA and GCTO.

  • Collaborates with the USMA Field Medical Alignment Director to ensure consistent standards, processes, and harmonization for training activities (e.g. clinical immersions, verbalizations, journal clubs, etc.)

  • Provides input into strategic congress priorities for USMA and participates in planning of RMSD activities at key scientific congresses; ensures alignment and pull-through of pre- and post-congress regional training and content needs

  • Represents USMA in partnership with GMA and GCSA in implementation of Input forums (SIEs, EIFs, GTEFs or Ad boards) as needed

  • Represents USMA as core member of Global Medical Communications Team (GMCT) to discuss and align on strategic context of emerging data, key communication points, probing questions for scientific engagement and training for execution pull through.

Minimum Education Requirements:

  • An advanced degree (M.D., Ph.D. or Pharm.D.), that is relevant to the TA specific disease area and recognized medical expertise in the TA.

Required Experience and Skills:

  • 5 years medical affairs experience or equivalent clinical/research experience; field medical affairs experience preferred

  • 3 years working in TA (clinical, research, or pharmaceutical environment) or within a highly relevant therapeutic area with demonstrated scientific acumen

  • Demonstrated ability to interpret and execute scientific strategy and to clearly articulate complex scientific concepts in 1:1 and group settings

  • Prior experience leading complex projects with demonstrated ability to handle multiple projects and priorities simultaneously and function in a fast-paced environment

  • Demonstrated ability to work in a complex organizational environment and ability to effectively operate in a team-oriented structure; promotes inclusion, maintains trust, and respects others

  • Excellent relationship and networking skills to effectively work across a heavily matrixed organization

  • Knowledge of US Healthcare system, national and society treatment guidelines, clinical research processes, FDA regulations, and OIG guidelines

  • Strong interpersonal, verbal, and written communication skills, proficient in Word, PowerPoint, and Excel

Preferred Experience and Skills:

  • University level teaching experience

  • Quickly and comprehensively learns about new subject areas and environments

  • Works well independently across several projects and addresses complex problems with discipline

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

Who we are …

We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

What we look for …

In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.

Invent. Impact. Inspire.

NOTICE FOR INTERNAL APPLICANTS

In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.

If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.

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.

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


EEOC Poster

EEOC GINA Supplement​

OFCCP EEO Supplement

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. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Remote Work

Shift:

Valid Driving License:

Hazardous Material(s):

Number of Openings:

1

Requisition ID:R108517