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Senior Director, Trials and Research Excellence (TREX)

AT Johnson & Johnson
Johnson & Johnson

Senior Director, Trials and Research Excellence (TREX)

Antwerpen, Belgium

Johnson and Johnson is currently seeking a Senior Director, Trials and Research Excellence located in Raritan, NJ; Basil, Switzerland or Beerse, Belgium.

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/.

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For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The Senior Director, Trial Research Excellence (EMEA+AP) is responsible for driving delivery of Worldwide Integrated Evidence Generation Plans and studies, through the design and implementation of aligned worldwide processes, standards and governance. This role will work in partnership with Medical Affairs Delivery Unit (MADU) to optimize J&J Medical Affairs Research activities. As 65% of WWIEGP is operationalized outside of the Americas, this role will focus on WW IEGP conducted in the EMEA and AP regions and act as the lead liaison with MADU leadership based in Basel, Switzerland.

TASKS / DUTIES / RESPONSIBILITIES

Work closely with Head of IEGP to develop and implement worldwide processes, standards, and templates in collaboration with Market Access, MADU, and Real-World Evidence, across global/regions/countries.

• Design, implement and maintain, in collaboration with cross functional and regional partners, WW Research Standards, processes, and templates for strategy and planning of Interventional & Non-Interventional Prospective Medical Affairs Research Studies.

• Support implementation of WW Standards through partnership with disease area aligned Medical Affairs Research Teams (MARTs) and input to the supporting operating model

• Oversee best in class cross-TA evidence generation strategy for WW IEGP

• Establish WW Evidence Generation 10yr analysis anticipating future product approvals. Identify and collate with key stakeholders (TA VPs, GMALs, TAMALs, regional MAF TA leads) a core set of evidence deliverables and associated timelines that will create WW value.

• Design algorithm and metrics to track and communicate medical and business impact of WW IEGP.

• Strengthen engagement and processes with key regions and countries in EMEA+AP and

facilitate early dialogue as a WW EG community

Enabling Capabilities

• In partnership with GMAF IT and GMAF Strategic Operations, be WW IEGP liaison for WESS system to track end-to-end WW MAF Research

• Ensure solution development and successful implementation through roll out of relevant training to J&J Medical Affairs Worldwide

Continually assess the need for new organizational capabilities or resources to effectively support cross-TA evidence strategy development

Governance

• Optimize WW IEGP prioritization criteria and assessment process

• Design and implement end-to-end MAF Research Governance and processes

Partner with MADU to create metrics to monitor IEGP study milestones and ensure studies conducted to optimal speed and cost efficiency

Qualifications

• Minimum of a Bachelor's degree

• 3 years of people management experience with a proven ability to achieve results through others

• 10 - 12 years of relevant experience in a medical/clinical or scientific environment/ pharmaceutical experience

• Previous experience leading clinical trials, developing and executing evidence generation plans and building medical strategies

  • Demonstrated leadership ability to successfully work across functional and geographic boundaries, preferably across multiple countries/market types/access models is required.
  • Strong collaboration/matrix management, influencing, strong communication skills (both written and oral)

• Process excellence, project management and strong organizational skills is preferred

  • Demonstrated learning agility and the ability to effectively influence portfolio strategies based on insights and foresights to future scientific direction is required
  • Understanding of Pharma R&D process in high innovation environment is required
  • Proven strategic thinking and strategic commercial skills across product and lifecycle is required

• Global mindset with proven ability to partner cross culturally and regionally is required

• Ability to drive projects forward to completion through planning and organizational skills while maintaining focus on the long-term strategy is required

• 20% Travel domestically and internationally

• Minimum of 3 years people management experience

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.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.

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

Eligible for benefits to include medical, dental, vision and time off as well as any others as provided for in the applicable Collective Bargaining Agreement.

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

Client-provided location(s): Antwerp, Belgium; Switzerland; Raritan, NJ, USA
Job ID: Johnson&Johnson-2406227346W
Employment Type: Other