Senior Director, Evidence Generation & Clinical Strategy

Job Function:

Marketing

Job Sub Function:

Strategic Marketing

Job Category:

People Leader

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

Johnson & Johnson is currently seeking the best talent for a **Senior Director, Evidence Generation & Clinical Strategy **to join our MedTech Electrophysiology organization. This position will be based in Irvine, CA.

The Senior Director, Evidence Generation & Clinical Strategy will lead the Electrophysiology (EP) Evidence Generation Strategy (EGS) process, ensuring evidence generation priorities are aligned to business strategy, portfolio objectives, clinical needs, regulatory requirements, and market access opportunities. The role serves as the primary orchestrator of the annual and quarterly evidence planning process, collecting, consolidating, and prioritizing evidence needs from business partners across Global Strategic Marketing Upstream and Downstream, Regional Marketing, Clinical Research, Medical Affairs, Regulatory Affairs, Health Economics & Market Access, Strategy, and R&D. This role partners closely with Clinical Science & External Research (CSER).

This highly strategic leadership role drives cross-functional alignment on evidence generation priorities and translates commercial, clinical, and competitive insights into an actionable evidence agenda. The position acts as the primary bridge between business partners and CSER, ensuring evidence plans are aligned with portfolio priorities, launch readiness, long-range financial planning, and annual business planning cycles.

This candidate should possess deep knowledge of EP therapies, clinical evidence requirements, product strategy, portfolio management, and regulatory pathways, with proven ability to influence senior leaders and drive alignment across a complex organization. Additional responsibilities will include:

• Own and lead the annual Evidence Generation Strategy (EGS) process integrated with the Business Planning cycle.
• Lead structured evidence needs collection across GSM, Regional Marketing, Clinical Research, Medical Affairs, Regulatory Affairs, HEMA, Strategy, R&D, and CSER partners.
• Collect, organize, and synthesize evidence requests into a unified portfolio of strategic evidence needs across products, therapies, regions, and customer segments.
• Design and facilitate evidence prioritization processes that evaluate business impact, timing, customer value, regulatory significance, and strategic importance.
• Deliver prioritized evidence generation recommendations and investment proposals to senior leadership.
• Partner with CSER to translate prioritized evidence needs into integrated evidence plans and study portfolios.
• Serve as business owner for evidence governance, request templates, intake processes, prioritization criteria, and business partner alignment mechanisms.
• Lead quarterly reviews of emerging evidence needs and facilitate pathways for urgent requests requiring leadership review.
• Ensure evidence priorities align with LRFP objectives, new product introductions, indication expansion strategies, and portfolio priorities.
• Provide regular reporting to senior leadership regarding evidence priorities, plan status, risks, and expected data availability.
• Partner with Clinical and Medical Affairs teams to shape clinical study strategy and identify endpoints aligned with strategic business and market needs.
• Translate clinical evidence, trial data, and real-world outcomes into strategic insights that inform portfolio and commercialization decisions.
• Collaborate with Regulatory and Medical Affairs to ensure evidence plans support future claims, market access, and regulatory requirements.
• Serve as an internal authority on EP trends, guidelines, ablation technologies, mapping systems, and competitive evidence strategies.
• Help own the strategy for white papers, KOL engagement, conference planning, and thought leadership activities supporting long-term evidence objectives.
• Engage with electrophysiologists, key opinion leaders, professional societies, and external partners to identify emerging evidence opportunities and gaps.
• Contribute to publication strategies, podium presence, and major EP conferences (e.g., HRS, EHRA, APHRS).
• Support new product launches and market expansion through evidence-backed differentiation and value creation strategies.
• Lead, coach, and develop a high-performing Evidence Generation & Clinical Strategy team.
• Monitor the competitive landscape, emerging technologies, and clinical developments to identify future evidence opportunities.
• Perform other duties as assigned.

Qualifications:

• Bachelor's degree in Life Sciences, or related field required. Advanced degree (MBA, MSc, MPH, PhD, or equivalent) preferred. MD profiles would be strongly considered.
• 15+ years of relevant business experience in Clinical Marketing and Strategy, or related fields. MD profiles coming from field of EP can apply without prior business experience.
• Experience in medical devices and electrophysiology or cardiovascular markets required
• Proven ability to develop strategies based on clinical, market, competitive, and health economic evidence.
• Deep understanding of clinical trial processes, regulatory environments, and evidence generation planning.
• Experience translating clinical data into business strategy, commercialization planning, and portfolio decisions.
• Strong written and verbal communication skills, including experience supporting publications and scientific communications.
• Experience working with KOLs and supporting peer-reviewed publications or conference presentations.
• International/global marketing experience preferred.
• Ability to influence cross-functional partners and lead in a large, complex environment.
• Strong financial competence and understanding of business planning processes.
• Strong analytical skills with the ability to make data-driven decisions.
• Demonstrated experience leading complex prioritization, governance, or portfolio management processes.
• Ability to drive consensus among senior leaders across functions and geographies.
• Knowledge of EP portfolio strategy, product lifecycle management, and evidence planning preferred.

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at [https://www.jnj.com/medtech](https://www.jnj.com/medtech).

Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.