Lead, Trial Delivery Management (Clinical Trials)

Location: Spring House, Pennsylvania, United States, or Titusville, New Jersey, United States. Additional country-specific postings are available in High Wycombe, United Kingdom; Beerse, Belgium; Breda, Netherlands; Warsaw, Poland; Madrid, Spain; and Milan, Italy. Travel up to 15–20% may be required.

Base pay: $109,000–$174,800 per year.

Company

Johnson & Johnson develops healthcare, pharmaceutical, and MedTech solutions, including innovative medicines and clinical treatments.

What you will do

• Execute study-level activities and create or update trial-specific documents, including monitoring guidelines, informed consent forms, and investigational medicinal product documentation.
• Set up and manage study vendors, including statements of work, budgets, and daily delivery activities.
• Coordinate country and regional trial management activities, feasibility strategies, target setting, and local risk reviews.
• Support compound training and contribute to trial-level operational strategies with Clinical, CTL&D, and Medical Writing partners.
• Resolve trial-related issues, develop risk mitigation plans, and support health authority inspections.
• Improve processes across trials and programs while mentoring and supporting new Trial Management team members.

Requirements

• Bachelor of Science degree or equivalent, preferably in Life Sciences such as Biology, Chemistry, Biochemistry, Nursing, or Pharmacy.
• At least 4 years of clinical trial experience in the pharmaceutical, healthcare, or related industries.
• Operational knowledge across Phase I–IV studies and experience managing multiple aspects of clinical trial execution.
• 2–3 years of experience supporting multiple aspects of global clinical trials.
• Leadership, analytical decision-making, financial management, project planning, communication, and presentation skills.
• Experience working in multifunctional matrixed environments, leading without authority, mentoring others, and operating with limited supervision.

Nice to have

• Experience in pharmaceutical, biopharmaceutical, or biotechnology industries.
• Knowledge of Clinical Trial Management Systems, clinical trial design, laboratory operations, quality assurance, regulatory compliance, and Standard Operating Procedures.

Culture & Benefits

• Inclusive work environment focused on individual contributions, diversity, and dignity.
• Retirement pension and 401(k) savings plans.
• Eligibility for a long-term incentive program.
• Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.