Johnson & Johnson

Sr. Manager, Trial Delivery Leader (1 of 8)

Johnson & Johnson$137K — $235K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) required.
  • 8+ years in Pharmaceutical, Healthcare or related industries.
  • 2+ years leading global clinical trials.
  • Operational knowledge across multiple phases of studies (Phase I-IV).
  • Proven leadership skills and ability to foster team productivity.
  • Experience in multi-functional, matrixed global environments.
  • Strong decision-making, analytical, and financial management skills.

Responsibilities

  • Lead Cross Functional Trial Team (CFTT) to execute trial operational plan.
  • Ensure overall trial delivery meets budget, timelines, and quality standards.
  • Identify and mitigate risks to ensure timely trial completion.
  • Ensure compliance with health authority regulations and internal procedures.
  • Participate in Health Authority inspections and internal audits.
  • Collaborate with R&D Quality for consistent inspection readiness.
  • Support process improvement initiatives at various organizational levels.

Benefits

  • Participate in consolidated retirement plan and savings plan (401(k)).
  • Eligible for long-term incentive program.
  • 120 hours of vacation annually.
  • Up to 40 hours of work, personal, and family time per year.
  • 480 hours of parental leave within one year of a child's birth/adoption/foster care.
  • Bereavement leave for immediate and extended family members.
  • Volunteer leave of 32 hours annually.
Full Job Description
Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Project Management

Job Category:
People Leader

All Job Posting Locations:
La Jolla, California, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job Description:

Please 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):

Canada: R-093251

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

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

This is a remote/hybrid 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.

We are searching for the best talent for a Sr. Manager, Trial Delivery Leader.

Purpose:

The Sr. Manager, Trial Delivery Leader (TDL) is accountable for clinical trial delivery, providing operational oversight of cross-functional deliverables. The TDL leads a cross-functional team trial team to build and deliver the trial operational plan, identifying and mitigating risks to effectively deliver assigned trials on time, on budget and in a compliant manner.

You will be responsible for:
  • Responsible for leading the Cross Functional Trial Team (CFTT) to influence and execute delivery
  • of the operational plan and for end-to-end trial execution.
  • Accountable for overall trial delivery, budget, timelines, quality, and milestones (e.g., support
  • DBL / CSR / TLR planning and scope, define protocol deviations and resolution pathways).
  • Proactively ensure that trial deliverables and milestones are met.
  • Identify risks and ensure mitigation and contingencies are being initiated and followed through.
  • Ensure trial is operationalized in compliance with global health authority regulations and
  • guidelines and internal operating procedures and processes.
  • Accountable for identifying risks in study conduct, developing mitigation plans and escalating
  • concerns to the CT or CDT.
  • Participate in preparation for, and conduct of, Health Authority inspections and internal QA
  • audits.
  • Ensure that the trial team operates in a constant state of inspection-readiness, collaborating
  • with R&D Quality to ensure quality oversight.
  • Participate in process improvement activities at a trial, compound & cross-DU level, as needed.


Additional Responsibilities may Include:
  • Lead and ensure inspection readiness for program through risk identification and readiness
  • review.
  • Provide leadership 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.


Qualifications / Requirements:

Education: Bachelor's degree is required. Preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).

Required:
  • Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
  • Minimum 2 years' experience leading multiple aspects of a global clinical trial.
  • 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.
  • 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.
  • Travel up to 15-20% of the time, defined by business needs


Required Skills:

Preferred Skills:
Budgeting, Clinical Trial Designs, Clinical Trials, Compliance Management, Contract Management, Developing Others, Execution Focus, Fact-Based Decision Making, Inclusive Leadership, Laboratory Operations, Leadership, Process Improvements, Productivity Planning, Project Integration Management, Research and Development, Research Ethics, Resource Planning, Team Management

The anticipated base pay range for this position is :
$137,000.00 - $235,750.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Company's 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: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

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At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

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Leverage Johnson & Johnson’s culture of innovation to transform health care and improve the lives of people around the world. Our collaborative environment encourages leadership and growth, allowing you to pioneer new strategies for health care solutions with a diverse team of experts.

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Engage in groundbreaking work that enhances how care is delivered on a global scale. Johnson & Johnson’s commitment to innovative health solutions results in dynamic career paths filled with opportunities for professional growth and development.

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Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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