About the role

The Manager of Trial Delivery Management is responsible for the execution of study-level activities, including vendor oversight, budget management, and the creation of critical trial-specific documentation. They also coordinate regional operational delivery, align feasibility strategies, and mitigate risks to ensure successful clinical trial outcomes.

What they look for

Clinical Trial Management Project Management Vendor Management Budget Oversight Risk Management Pharmaceutical Development Leadership Analytical Reasoning Communication Presentation Skills Mentorship Process Improvement Compliance Management Clinical Research Contract Management Technical Credibility

Requirements

Candidates must hold a Bachelor's degree in a Life Sciences field and possess a minimum of 8 years of experience in the pharmaceutical or healthcare industry. The role requires proven leadership skills, extensive knowledge of clinical research across multiple phases, and the ability to operate effectively in a global matrixed environment.

Full description

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:

Remote (US)

Job Description:

Position Summary:

The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities. The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.

Principal Responsibilities:

Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).

Vendor set up and management of day-to-day study vendor activities, including set-up, SOW creation and budget oversight.

Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform country-level risk reviews, aware of all projects conducted across countries).

Support development of program-level compound training, collaborating with Clinical / CTL&D Medical writing.

Additional Responsibilities may Include:

Provide input into trial level operational strategies.

Resolve trial-related issues and mitigate trial-related risks.

Participate in process improvement activities at a trial, compound & cross-DU level, as needed.

Provide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues.

Mentor & support onboarding of new team members, particularly those in Trial Management.

Foster employee engagement, inclusion, and Credo Behaviors.

Principal Relationships:

Internal: Trial Management Directors, Clinical Trial Leaders, Clinical Trial Assistants, Representatives of

Delivery Operations, representatives of other GD Functions and Clinical Teams, representatives of

Procurement

External: Vendors

Education and Experience Requirements:

Required Minimum Education:

BS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)

Required Years of Related Experience:

Minimum of 8 years in Pharmeceutical, Healthcare or related industries.

Required Knowledge, Skills and Abilities:

Experience in and knowledge of the pharmaceutical development process.

Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV); must have the ability to manage all aspects of execution of a clinical trial.

2-3 years’ experience leading multiple aspects of a global clinical trial

Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness.

Experience of leading without authority and in muti-functional matrixed and global environments.

Excellent decision-making, analytical and strong financial management skills are essential to this position.

Operate and execute with limited supervision.

Experience mentoring/coaching others.

Strong project planning/management, communication and presentation skills are required.

Required Skills:

Preferred Skills:

Analytical Reasoning, Budgeting, Clinical Trial Management Systems (CTMS), Clinical Trials, Compliance Management, Contract Management, Execution Focus, Fact-Based Decision Making, Laboratory Operations, Mentorship, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Standard Operating Procedure (SOP), Technical Credibility