Global Senior Strategic Evidence Director, Trial Research Excellence
Join a forward-thinking organization to lead the delivery and scientific business impact of worldwide integrated evidence generation plans and studies. This role involves driving the design and implementation of aligned processes, standards, and governance across global regions.
The ideal candidate will have a strong background in clinical trials, evidence generation, and medical strategy. They should be able to develop and execute evidence generation plans, build medical strategies, and collaborate with cross-functional teams.
* Design, implement, and maintain worldwide research standards, processes, and templates for strategy and planning of Interventional & Non-Interventional Prospective Medical Affairs Research Studies.
* Support the implementation of worldwide standards through partnership with disease area-aligned medical affairs research teams (MARTs) and input to the supporting operating model.
* Oversee best-in-class cross-therapeutic area evidence generation strategy for worldwide integrated evidence generation plans.
* Establish a 10-year analysis anticipating future product approvals, identify, and collate with key stakeholders core sets of evidence deliverables and associated timelines that create worldwide value.
* Design algorithms and metrics to track and communicate medical and business impact of worldwide integrated evidence generation plans.
Required Skills and Qualifications:
* A minimum of a Master's degree in a scientific or related discipline is required; an advanced scientific/medical degree (PhD, PharmD, or other advanced degree) is preferred.
* At least 10-14 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 learning agility and the ability to effectively influence portfolio strategies based on insights and foresights to future scientific direction.
* Proven strategic thinking and commercial skills across product lifecycle.
* Ability to drive projects forward to completion through planning and organizational skills while maintaining focus on the long-term strategy.
* Demonstrated leadership ability to successfully work across functional and geographic boundaries, preferably across multiple countries/market types/access models.
* Strong collaboration/matrix management, influencing, communication skills (both written and oral).
* Process excellence, project management, and strong organizational skills are required.
* Understanding of Pharma R&D process in high innovation environments is required.
* Global mindset with proven ability to partner cross-culturally and regionally is required.
Benefits:
This position is eligible to participate in the company's consolidated retirement plan (pension) and savings plan (401(k)). Additionally, employees may be eligible to participate in the company's long-term incentive program and time-off benefits, including vacation, sick time, holiday pay, and personal/family time.
Others:
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, or protected veteran status. The company actively seeks qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.