Johnson & Johnson

MSL Field Director, Caplyta - Northeast

Johnson & Johnson$164K — $282K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree required; PharmD, PhD, or MD preferred.
  • Minimum of 8 years in related fields, with at least 4 years of pharma industry experience and 2 years as an MSL.
  • Previous management experience essential for leading a team.
  • Experience in therapeutic areas related to neuroscience preferred.
  • Strong analytical skills for data gathering and strategic thinking required.

Responsibilities

  • Lead the Caplyta MSL team to enhance scientific engagement in the region.
  • Develop and execute regional strategy with measurable objectives and priorities.
  • Conduct coaching and development of MSLs, emphasizing performance improvement and career growth.
  • Oversee execution of Medical Affairs programs, ensuring alignment with objectives.
  • Collaborate with cross-functional teams to deliver on scientific goals and strategies.

Benefits

  • Eligible for consolidated retirement plan and 401(k).
  • 120 hours of vacation per year, plus additional sick time.
  • Up to 13 holidays per year, including floating holidays.
  • Provide various leave options including parental, bereavement, and caregiver leave.
  • Opportunity for volunteer leave and support for military spouses.
Full Job Description
Job Function:
Medical Affairs Group

Job Sub Function:
Multi-Family Medical Affairs

Job Category:
Professional

All Job Posting Locations:
Connecticut (Any City), Delaware (Any City), Maine (Any City), Maryland (Any City), Massachusetts (Any City), New Hampshire (Any City), New Jersey (Any City), New York (Any City), Rhode Island (Any City), Vermont (Any City), Virginia (Any City), West Virginia (Any City)

Job Description:

Johnson & Johnson Innovative Medicines is recruiting for a MSL Field Director, Caplyta to be based in the Northeast territory which includes: Maine, New Hampshire, Vermont, Massachusetts, Rhode Island, Connecticut, New York, New Jersey, Pennsylvania, Delaware, Maryland, Virginia, and West Virginia.

About Therapeutic Area

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Neuroscience team tackles the world's toughest brain health challenges including multiple sclerosis, Alzheimer's disease, Parkinson's disease, myasthenia gravis, epilepsy, major depressive disorder, bipolar disorder, schizophrenia, and autism. This patient-focused team helps address some of the most complex diseases of our time.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Position Summary

The Field Director is responsible for leading the Caplyta US Northeast Medical Science Liaison (MSL) team in providing scientific, clinical, research, and educational support to health care professionals and internal partners related to Caplyta, while ensuring customer centric, insight driven, and compliant scientific engagement across the region.

The Field Director will partner with the MSL Head to set and drive strategy for their region/organized providers, translating TA and Medical Affairs strategy into clear regional priorities, measurable objectives, and executional excellence. The Field Director is responsible for ensuring strong clinical engagement strategy for each territory within their region and will conduct routine strategy reviews with each MSL direct report, leveraging data, insights, AI tools, and performance trends to guide decision making.

The primary role of the Field Director is to provide support, coaching, and development to each of their direct reports (MSLs), utilizing the skills framework, routine feedback, and periodic field observation, with a strong emphasis on strength-based coaching, continuous improvement, and career development planning.

The Field Director will be responsible for the execution of field Medical Affairs programs, including product launches, proactive initiatives, and HCP engagement. The Field Director is responsible for ensuring that each direct report is functioning at the expected level of scientific acumen/expertise, presentation skills, and soft skill abilities, including professional credibility and command, stakeholder influence, adaptive communication, and effective scientific storytelling. In addition, the Field Director plays a critical role to remove barriers and aligning field activities to ensure impactful scientific engagement.

The Field Director is responsible for staying abreast of scientific information and disease states to ensure proficient interaction model, and coach with their team. They will also ensure their direct reports execute collection and analysis of high quality, actionable Medical Insights and effectively communicate them to inform strategy, evidence generation, and lifecycle planning.

The Field Director will demonstrate effective change leadership by upholding professionalism, performance, and integrity in challenging situations, and by guiding the team with resilience, accountability, and engagement through ambiguity and shifting priorities.

The Field Director will coordinate closely with Medical Affairs, Scientific Affairs, and cross functional partners to align objectives and execution as appropriate. The Field Director is expected to identify possible solution(s) and make a recommendation to the MSL Head for action, demonstrating strong critical thinking, risk assessment, and sound judgment. The recommendations are expected to support the company's scientific objectives. In addition, the Field Director will work collaboratively with local and regional internal business partners to meet scientific needs of customers, acting as a trusted scientific leader and strategic thought partner.

The Field Director is responsible for providing oversight of all activities in accordance with current regulatory and health care compliance guidelines, modeling compliant behavior, reinforcing ethical decision making, and ensuring a culture of accountability and integrity across the team.

Regional Team Leadership Responsibilities
  • Responsible for the management of a regional MSL team including:
  • Ensure that team functions according to the business plan and company directives.
  • Drive team performance through regular field visits and 1:1s, providing observation, coaching, and timely, candid, and constructive feedback aligned to performance expectations, development goals, and career progression.
  • Provide oversight responsibility for team's training and development, ensuring ongoing scientific, skills based, and leadership capability building.
  • Ensure team optimal capacity, field activity level, and field metrics, using data and dashboards to monitor performance and drive continuous improvement.
  • Models and develop teams' scientific exchange skills to elevate the quality and impact of medical engagement across the organization, ensuring appropriate objection handling and correction of misperceptions and inaccuracies.
  • Ensures each MSL territory plan is strategic, up to date and actionable.
  • Manages the team through special projects and cross-functional support activities, balancing workload, priorities, and development.
  • Recruit, Retain, and develop a diverse high-performing team by implementing inclusive leadership strategies to inspire and motivate their team members, championing diversity, equity, inclusion, and belonging in all hiring and talent decisions.
  • Provide career and succession planning in support of staff reaching their highest potential with identification of high potential talent and readiness planning.
  • Provide an optimal working environment grounded in Credo values by communicating of a clear direction, active listening, respecting diversity, encouraging collaborative partnership, empowering direct reports, follow up on commitments, promoting innovation, and rewarding high performance, while fostering trust and accountability.
  • Responsible for timely completion of administrative duties, including assessment and approval of expense reports, preparation and communication of team metric reports, compliance documentation, and operational reporting.
  • Co-lead the communication of MSL team achievements, insights, and impact to appropriate internal partners and leadership, reinforcing value delivered by the field medical organization.


Cross Functional Collaboration & Scientific Leadership
  • The Field Director will serve as a leader and role model for compliant, effective cross-functional collaboration across their respective regions, ensuring routine, high-quality communication with field partners (e.g., Specialists, District Managers, KAMs, Clinical Educators, and MSL peers) in alignment with Medical Affairs strategy and customer needs.
  • Participate in business planning activities as necessary across the various brands and within Medical Affairs. Ensure appropriate training on and execution of proactive initiatives and other permissible field activities, ensuring alignment with Medical Affairs strategy and customer needs.
  • Partner with the MSL Head to develop and execute their region / organized provider strategies, providing field insights from KOLs and specialists to inform TA strategy, identify emerging trends and unmet needs, and support evidence generation opportunities.
  • Lead assigned scientific projects and programs with joint strategic design with the MSL Head and independent tactical execution. Demonstrate strong project management, prioritization, execution discipline, and effective translation of field intelligence into strategic recommendations for internal stakeholders.
  • May be responsible for identifying and developing field scientific strategies, aligned to TA medical priorities and lifecycle needs.
  • Participates and/or leads cross functional/company initiatives, representing Field Medical with credibility, influence, and strategic perspective.
  • Champions a culture of excellence by establishing scalable, high-impact processes that foster alignment, enhance efficiency, garner buy-in, drive compliance, and empower cross-functional teams to achieve shared goals.


Qualifications
  • A minimum of a master's degree is required. PharmD, PhD, MD highly preferred.
  • Minimum of 8 years required.
    • A minimum of 4 years of pharmaceutical industry, and a minimum of 2 years of MSL experience are required. Clinical/research experience is preferred
  • Previous people management responsibility is required.
  • TA-related experience is preferred.
  • Proficiency in data gathering and analysis, clinical expertise, problem solving, interpersonal influence, and cross-functional collaboration strategic thinking and competitive landscape analysis.
  • Must live in their assigned region and in close proximity to an airport. This role requires regional travel of approx. 60% depending on geography (including overnight travel, periodic national scientific congresses and key strategic/scientific meetings at the corporate office in Horsham, PA/Titusville, NJ)
  • A valid US driver's license
  • Demonstrated commitment to learning emerging technologies, such as AI, through exploration, iteration, and applying new tools over time
  • Experience building team AI literacy and confidence, reinforcing trusted and responsible AI use and sound judgment


Required Skills:

Preferred Skills:
Analytical Reasoning, Business Planning, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trials Operations, Fact-Based Decision Making, Health-Medical Programs, Leadership, Medical Affairs, Medical Communications, Program Management, Regulatory Affairs Management, Strategic Thinking, Subject Matter Experts (SME) Collaboration, Tactical Planning, Technical Credibility

The anticipated base pay range for this position is :
$164,000.00 - $282,900.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company's long-term incentive program.

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation -120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year

Holiday pay, including Floating Holidays -13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave - 80 hours in a 52-week rolling period10 days

Volunteer Leave - 32 hours per calendar year

Military Spouse Time-Off - 80 hours per calendar year

The following link to general company benefits information MUST also be included in the posting: Please use the following language:

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
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141,700 employees
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$14.7 billion
Founded
1886
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+5.5%
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