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Merck Executive Director, US Field Medical Affairs, Health Systems Oncology in Topeka, Kansas

Job Description

Role Summary:

  • The primary role of the US Executive Director, Field Medical Affairs, Health Systems Oncology (EDFMA-HSO) is the leadership, management, and accountability of a team of US Field HSO Medical Affairs Directors (HSO MAD) and headquarters-based (HQ) HSO Payor & Access Strategy Leads (PASL) within US Medical Affairs (part of GMSA, Global Medical and Scientific Affairs).

  • The EDFMA-HSO serves as the primary leadership point to ensure successful coordination and execution of USMA field-based scientific and value evidence strategy across all Oncology products and in alignment with GMSA Value & Implementation (V&I) plans.

  • The EDFMA-HSO is accountable for all aspects of recruiting, hiring, on-boarding, and development of field medical affairs personnel in order to establish and implement field support for key decision makers (KDMs) within defined health care organizations. In addition, the EDFMA-HSO collaborates with Outcomes Research, Clinical Development, Global Human Health (GHH), EDFMA Health Systems, EDFMA of Oncology TA teams, Global Medical & Value Capabilities (GMVC), and US Regional Directors Medical Affairs (RDMA) to align on HSO Field Execution Plans (FEP). The EDFMA-HSO is accountable for ensuring field teams execute on FEPs and achieve field execution metrics.

  • The EDFMA-HSO is accountable for employee performance management, organizational talent review, development plans, and succession planning. The EDFMA-HSO will report directly to the Associate Vice President (AVP) and Head of USMA Health Systems.

Primary Responsibilities:

Leadership and Management

  • Provide ongoing assessment of HSO TLs and HSO PASLs, supports implementation of individualized employee development priorities and key performance indicators (KPIs), and completes performance evaluations based on observations, deliverables, and feedback from peers and customers.

  • Provide guidance to the HSO TLs to ensure compliant field medical activities that support the safe, effective, and knowledgeable use of Company products.

  • Collaborate with EDFMAs for various therapeutic areas (TAs) to ensure the sharing of best practices and cross-collaboration amongst the different TA field teams and HSO field team members.

  • Supervise HSO TL management of field medical teams to meet the following objectives:

  • Execute on regional and territory scientific exchange FEPs

  • Support USMA scientific exchange activities and meetings with KDMs at scientific congresses

  • Maintain relationships with KDMs essential to insight collection.

  • Identify new and emerging changes in the health care environment in areas of importance to our company

Strategic Planning and Project Management

  • Ensure external insights are evaluated and integrated into V&I and other relevant scientific platform development to inform strategic planning with the goal of creating tactics that are actionable and achievable by the HSO Field team.

  • Incorporate Scientific Platform, including insights from KDMs, with execution of Field Medical strategy and tactics.

  • Optimize HSO team alignment, integration, and tactical implementation via coordination with the field medical leadership team and HQ Medical Affairs teams.

  • Assist AVP and Head of US Health Systems with field medical strategic planning and resource management related to KDMs and IDNs.

  • Provide strategic input into development of V&I plans and ensure development and implementation of bi-annual Field Execution Plans (FEP) that are strategically aligned with V&I plans.

  • Ensure proper resourcing and flawless execution of FEPs by field teams via KPI tracking and quarterly impact reporting.

Internal Collaboration and Alignment

  • Actively and effectively interface with appropriate Outcomes Research, Clinical Development, Commercial (GHH), GMVC teams and TA leadership including Executive Directors of Medical Affairs (EDMAs), Global Directors of Medical Affairs (GDMAs) and US RDMAs

Budget Management

  • Oversee the development and effective management of the team’s budget.

  • Oversee and ensure appropriate approval of key travel decisions, congress participation, and expense approvals, as applicable and appropriate.

  • Oversee field medical affairs activities and ensure budgets are in alignment with priorities so that proposed vs. actual budgets are aligned

Education:

  • Advanced healthcare/science degree (MD, PhD, or PharmD)

Required Experience and Skills:

  • Individual with demonstrated ability to effectively lead and coach scientific colleagues at all skill and knowledge levels and with a strong working knowledge of US healthcare delivery systems, managed markets, health economics, outcomes research, and health care quality

  • 10+ Pharmaceutical Industry or equivalent experience and minimum of 5+ years of field medical front-line management experience in the pharmaceutical industry

  • Demonstrated learning agility and experience managing medical teams

  • Ability to effectively engage senior management to implement field medical vision and strategies.

  • Strong understanding of the healthcare ecosystem, access decision-making and account planning/management.

  • Excellent interpersonal, communication, and presentation skills, strong personal integrity, teamwork and collaboration abilities, strong business and financial acumen, and customer focus are necessary.

  • A thorough understanding of the FDA, OIG, anti-kickback, and other ethical guidelines relevant to the pharmaceutical industry, and demonstrated history of ensuring field medical compliance with external and internal guidelines and standard operating procedures.

  • Must be able to organize, prioritize, and work effectively in a constantly changing, ambiguous environment and to motivate a team to do the same.

  • Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, and Office of the Inspector General (OIG), Health Insurance Portability and Accountability Act (HIPAA), and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its external stakeholder environment

  • Ability to travel across assigned area. Estimated travel 50%.

Preferred Experience and Skills:

  • 5 years of direct field medical management responsibilities within the pharmaceutical industry

  • Strong working knowledge of the Microsoft Office Suite (Word, PowerPoint, Excel), Veeva, and other systems used by field medical teams.

  • Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of scientific insights.

Location :

  • UG (PA) or Rahway (NJ) – HQ strongly preferred

  • Relocation not available

Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)

Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

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 (https://survey.sogosurvey.com/r/aCdfqL) 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:

EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)

EEOC GINA Supplement​

Pay Transparency Nondiscrimination (https://www.dol.gov/sites/dolgov/files/OFCCP/pdf/pay-transp_%20English_formattedESQA508c.pdf)

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.

Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)

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:

$250,800.00 - $394,800.00

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 (https://www.benefitsatmerck.com/) .

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

50%

Flexible Work Arrangements:

Remote

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

02/10/2025

*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: R333311

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