At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
We are seeking a Director, Global Medical Affairs Strategy & Execution in Oncology.
Primary Responsibilities include, but are not limited to:
The Director, Global Medical Affairs Strategy & Execution collaborates with the Global Medical Affairs Leaders (GMAL) to support the strategic objectives of the Global Medical Affairs function. The Director, Global Medical Affairs Strategy & Execution will partner with the GMAL in one or more designated Therapeutic Areas/Products to own the strategy and execution of the Global Medical Affairs Function, including:
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• Generation of an Integrated Evidence Generation Plan (IEGP) that meets prioritized regional needs
• Facilitate Worldwide Medical Affairs Strategy Team (W-MAST) meetings
• Lead and implement the publication strategy/global publication plans
• Identify strategies to gain external insights strategies (advisory boards, pre/post congress meetings, etc.)
The Director, GMA Strategy & Execution is accountable for:
• Global Medical Affairs Owned Cross-Pharma Policies and SOPs, such as Research Concept Approval Process and System, Publication SOP and System, Investigator-Initiated Studies Policy, Collaborative Studies, Methods Review, Etc.
• Global Medical Affairs strategy and business planning process
• Integrated Evidence Generation Plan
• Global publication planning process
• Global Medical Affairs Operating Model
• Global Medical Affairs SharePoint Site Management/Scientific and Knowledge Information Management
• Global Medical Affairs Procurement Operating Procedure
• GCSO Advisory Board Business Operating Procedure
Essential functions:
- Co-lead with the Global Medical Affairs Leaders in preparing robust Integrated Evidence Generation Plans for compounds in development that reflect prioritized regional and local needs.
- Coordinate with the GMAL to lead the publications process. Ensure the development of publications follows the Cross-Pharma Publication SOP. Supervise publication vendors. Coordinate publication discussions in collaboration with agency partners and J&J colleagues. Maintain the relationship with editorial staff at key journals and key scientific and academic societies. Handle the publication review and workflow with vendor support.
- Oversee the successful implementation of the GMA Operating model via Worldwide Medical Affairs Strategy Team (W-MAST) to gain regional input and alignment.
- Manage the TA/Product GMA Budget and vendors.
- Lead all aspects of the Research Concept Approval Process for Medical Affairs studies. Ensure consistent implementation of the process and conducts due diligence activities.
- Frequent interactions with GMAL, Medical Affairs directors, Janssen R&D clinical scientists, global and regional marketing directors, regulatory leaders, outcomes research and statisticians. External interactions with key opinion leaders, academic institutions, medical organizations, agencies and consultants.
Qualifications
- A minimum of a BA/BS required. Advanced degree is preferred. Oncology experience is helpful.
Required Knowledge, Skills and Abilities:
- Minimum of 8 years of relevant experience required.
- Proven track record be a self-starter, goal oriented, possess excellent verbal and written communication skills, exceptional planning, and interpersonal skills, partnering, and problem solving.
- Must have the ability to multi-task and prioritize.
- Results & performance driven with strong negotiation and influencing skills.
- Demonstrated experience in managing and collaborating with internal/external partners, including outside consultants and vendors.
- Attention to detail with strong analytical skills required.
- Approximately 20% travel, both domestic and international, may be required.
- This position is based in Raritan, NJ. The ability to be in Raritan, NJ is required.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.
The anticipated base pay range for this position is $160,000 - $276.000.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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