Lead, Trial Delivery Management (1 of 3)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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:

Spring House Pennsylvania United States of America

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 note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s):

United States - Requisition Number: R-057753

Japan - R-059626

United Kingdom - R-059552

Switzerland - R-059564

Belgium France Netherlands Spain Italy Germany Poland - Requisition Number: R-059569

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

This is a remote role available in all states within the United States. While specific cities are listed in the Locations section for reference please note that they are examples only and do not limit your application. We invite candidates from any location to apply.

Remote work options may be considered on a case-by-case basis and if approved by the Company.

We are searching for the best talent for Lead Trial Delivery Management.

The Lead Trial Delivery Manager (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).

Manage 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.

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.

Required Minimum Education: Bachelors degree or equivalent preferred areas of study include Life Sciences (Life Sciences (e.g. Biology Chemistry Biochemistry Nursing Pharmacy).

Required Knowledge and Experience:

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

Minimum of 2 years experience supporting multiple aspects of a global clinical trial.

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

Experience 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.

Immunology clinical trial experience is preferred.

This job posting is anticipated to close on February 27 2026. The Company may however extend this time-period in which case the posting will remain available on to accept additional applications.

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 protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

#LI-Remote

Required Skills:

Preferred Skills:

Analytical Reasoning Clinical Research and Regulations Clinical Trial Designs Clinical Trial Management Systems (CTMS) Clinical Trials Communication Data Savvy Laboratory Operations Organizing Problem Solving Productivity Planning Professional Ethics Project Integration Management Quality Assurance (QA) Regulatory Compliance Research and Development Research Ethics Standard Operating Procedure (SOP)

The anticipated base pay range for this position is :

$109000.00 - $174800.00

Additional Description for Pay Transparency:

The expected base pay range for this position is $109000 to $174800.
The expected base pay range in the San Francisco Bay Area is $125000 to $201250.

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).



This position is eligible to participate in the Companys long-term incentive program.



Subject to the terms of their respective policies and date of hire employees are eligible for the following time off benefits:

Vacation 120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado 48 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year

Holiday pay including Floating Holidays 13 days per calendar year

Work Personal and Family Time - up to 40 hours per calendar year

Parental Leave 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave 80 hours in a 52-week rolling period10 days

Volunteer Leave 32 hours per calendar year

Military Spouse Time-Off 80 hours per calendar year

For additional general information on Company benefits please go to: -