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Johnson & Johnson

Manager, Trial Delivery Management

Johnson & Johnson

. Execute study-level trial delivery activities .

Posted 11/5/2026full-timeUnited StatesSeniorLead💰 $120,000 - $207,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in managing clinical trials, including execution, vendor management, and compliance oversight. Possesses strong leadership and project management skills, with a focus on fostering team productivity and collaboration in a global environment.

Highest-signal resume keywords
Clinical Trial ManagementPharmaceutical Development ProcessProject Planning/ManagementLeadership SkillsClinical Research Operational Knowledge

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ExecutionBudget OversightRisk ManagementSOP KnowledgeFeasibility Strategy AlignmentMonitoring Guidelines CreationInformed Consent FormsInvestigational Medicinal Product DocumentationContract ManagementLaboratory Operations
Soft Skills
Team ProductivityDecision-MakingAnalytical SkillsCommunication SkillsMentoring/Coaching
Tools & Technologies
Clinical Trial Management Systems (CTMS)
Industry Keywords
PharmaceuticalHealthcareClinical TrialsCompliance ManagementResearch Ethics

About the role

Key responsibilities & impact
  • Execute study-level trial delivery activities
  • Create and update critical trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and Investigational Medicinal Product documentation
  • Set up and manage vendors and day-to-day study vendor activities, including SOW creation and budget oversight
  • Coordinate and oversee country and regional trial management activities
  • Align feasibility strategy with local teams and perform country-level risk reviews
  • Support development of program-level compound training in collaboration with Clinical, CTL&D, and Medical Writing
  • Provide input into trial-level operational strategies
  • Resolve trial-related issues and mitigate trial-related risks
  • Participate in process improvement activities at trial, compound, and cross-DU levels
  • Support Health Authority inspections and identify program-level risks and mitigation plans
  • Mentor and support onboarding of new team members, particularly in Trial Management
  • Foster employee engagement, inclusion, and Credo Behaviors
  • Collaborate with Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Delivery Operations, GD Functions, Clinical Teams, and Procurement

Requirements

What you’ll need
  • BS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
  • Minimum of 8 years in Pharmaceutical, Healthcare or related industries
  • Experience in and knowledge of the pharmaceutical development process
  • Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV)
  • Ability to manage all aspects of execution of a clinical trial
  • 2-3 years’ experience leading multiple aspects of a global clinical trial
  • Excellent leadership skills and proven ability to foster team productivity and cohesiveness
  • Experience leading without authority and in multifunctional matrixed and global environments
  • Excellent decision-making, analytical, and financial management skills
  • Ability to operate and execute with limited supervision
  • Experience mentoring/coaching others
  • Strong project planning/management, communication, and presentation skills
  • Knowledge of Clinical Trial Management Systems (CTMS), clinical trials, compliance management, contract management, laboratory operations, research ethics, Standard Operating Procedures (SOP), and project integration management

Benefits

Comp & perks
  • Company benefits information provided at https://www.careers.jnj.com/employee-benefits
  • Hybrid work arrangement
  • Remote working considered on a case-by-case basis with business approval