Senior Local Trial Manager

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 jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

R&D Operations

Job Sub Function

Clinical Trial Project Management

Job Category

Professional

All Job Posting Locations:

Kibbutz Shefayim, Center District, Israel

Job Description

About Innovative Medicine

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.

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

About The Role

Johnson & Johnson is seeking a highly experienced Senior Local Trial Manager to join our Global Clinical Operations (GCO) team.

This is a senior clinical operations role responsible for the end-to-end management and oversight of clinical trials at the country level. The Lead Local Trial Manager serves as the primary local contact for assigned studies, ensuring high-quality execution from study start-up through closeout while maintaining compliance with protocol requirements, Good Clinical Practice (GCP), company procedures, and local regulatory standards.

The successful candidate will play a key role in leading local study delivery, driving operational excellence, mentoring colleagues, and collaborating with a broad range of internal and external stakeholders.

Key Responsibilities

• Lead and coordinate local clinical trial activities to ensure delivery of quality data, on time and within budget.

• Act as the primary country-level contact for assigned clinical studies.

• Support study feasibility and site selection activities in collaboration with cross-functional teams.

• Develop and implement local trial plans, recruitment strategies, risk mitigation plans, and contingency actions.

• Monitor study progress, identify risks, and implement corrective and preventive actions when needed.

• Ensure compliance with study protocols, GCP, local regulations, and company standards.

• Oversee local regulatory and ethics committee submissions and approvals.

• Collaborate with investigators, study coordinators, vendors, and cross-functional partners to drive successful study execution.

• Contribute to budget planning, forecasting, and financial tracking for assigned studies.

• Review study documentation, monitoring reports, site activities, and vendor deliverables.

• Support audits, inspections, and quality improvement activities.

• Mentor and coach clinical operations colleagues while contributing to capability-building initiatives and process improvements.

Qualifications

Required

• Bachelor's degree in Pharmacy, Nursing, Life Sciences, or another relevant scientific discipline.

• Significant experience in clinical trial management within the pharmaceutical, biotechnology, medical device, or CRO environment.

• Strong understanding of clinical development, ICH-GCP, and local regulatory requirements.

• Experience managing complex clinical studies and multiple priorities simultaneously.

• Demonstrated leadership, mentoring, and stakeholder management capabilities.

• Excellent communication and relationship-building skills.

• Ability to work effectively in a dynamic, fast-paced environment.

• Fluent in English and the local country language.

• Willingness to travel as required.

Preferred

• Therapeutic area expertise within one or more key disease areas.

• Experience leading cross-functional initiatives, process improvement efforts, or operational excellence programs.

• Experience leveraging digital and AI-enabled tools to improve productivity, decision-making, and study delivery.

What You'll Bring

• Strong project management skills

• Strategic thinking and problem-solving capabilities

• Ability to influence across diverse stakeholder groups

• Passion for delivering high-quality clinical research

• Commitment to patient safety, compliance, and operational excellence

About Johnson & Johnson

At Johnson & Johnson, we believe health is everything. Through innovation in healthcare, we are working to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and where solutions are personalized.

Join us and help bring life-changing healthcare innovations to patients around the world.

Required Skills

Preferred Skills:

Business Behavior, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trials, Communication, Give Feedback, Laboratory Operations, Medical Knowledge, Mentorship, Problem Solving, Process Oriented, Professional Ethics, Project Integration Management, Project Management, Research and Development, Research Ethics