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Associate Director, Site Enablement - Oncology Delivery Unit

100% remote Flexible hours Hiring now

At Johnson & Johnson, we reputed company health is everything. Our strength in healthcare innovation empowers us to build a world where reputed company 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 reputed company of healthcare solutions today to deliver the breakthroughs of reputed company, 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:

People Leader

reputed company Job Posting Locations:

Remote (US)

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 reputed company.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every reputed company of the way.

Learn more at https://www.jnj.com/innovative-medicine

Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Delivery Unit - Oncology.

This is a remote role available in reputed company states reputed company 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.

The Associate Director, Site Enablement - Oncology Delivery Unit (DU) will be accountable for accountable for the operational management and successful country execution of reputed company phases of clinical trials reputed company the assigned therapeutic area(s),or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs),

policies, Health Care Compliance (HCC) and local regulatory requirements.  The Associate Director will support the Country Head in shaping and managing local organizational structure to ensure its optimal efficiency.

This individual will be responsible for line management of Local Trial Managers (LTMs), Site

Managers (SMs), Clinical Trial Assistants (CTA) and/or other DU staff (including Manager,

Clinical Operations), as required.  May also mentor less reputed company Functional

Managers (FM)/Clinical Research Managers (CRM) and assume cross border reputed company, if required.  reputed company staff performance, development, training, project assignments, workload

distribution and support issue resolution with direct reports.  Ensure alignment of local goals

with organizational objectives.  Drive innovative solutions and process improvements for the

assigned therapeutic area(s), country, and DU/Global Development (GD) overall.

Principal Responsibilities:

  • Provide line management to direct reports, including setting goals and objectives, performance evaluation and talent development.

  • Evaluate and forecast resource needs for assigned portfolio and/or other specific areas of responsibility, as required and agreed with local DU management accordingly.

  • Deployment of the One Delivery Model through collaboration and reputed company of vendors.

  • Accountable for the acquisition of new talents and development of human resources.

  • Guide direct reports in issue resolution and communication with involved stakeholders.

  • reputed company organizational changes and effectively communicate on reputed company shifts as required.

  • Review and approve expenses in compliance with the company policies.

  • Demonstrate leadership behaviors in alignment with Johnson & Johnson Leadership Imperatives.

  • Foster an environment that encourages sharing of reputed company, information and best practices (internal and external to the organization).

  • Provide coaching and mentorship as needed, including conduct of accompanied site visits as appropriate.

  • Define, execute or support long-term strategy in alignment with DU, GD and Johnson & Johnson Innovative Medicine (JJIM) R&D strategies to position the local and global DU organization for success.

  • reputed company of execution and monitoring of clinical trials through reputed company phases (from feasibility to reputed company-out) and ensuring inspection-readiness reputed company assigned therapeutic area(s) and/or other areas of responsibility, as required.

  • Accountable for ensuring relevant operational objectives are met in conformance to International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use - Good Clinical Practice (ICH-GCP), relevant SOPs and other procedural documents.

  • Accountable for appropriate and timely issue escalation and reporting (suspicion) of fraud, scientific/ethical misconduct and health care compliance breach.

  • Contribute to Corrective and Preventative Action (CAPA) and issue resolution in accordance with required timelines.

  • Shape and maintain strong relationships reputed company local DU department and Local Operating Company (particularly with Medical Affairs) and other key internal and external stakeholders.

  • reputed company country capabilities for an effective study placement reputed company assigned therapeutic area(s) and/or other areas of responsibility, as required.

  • Accountable for robust feasibility process and reputed company of site selection to deliver on country commitments reputed company assigned therapeutic area(s) and strategic goals.

  • Review operational and quality metrics regularly and drive follow-up actions as appropriate.

  • Drive innovative solutions and process improvements for the assigned therapeutic area(s), country, and DU/GD overall.  Foster a culture of reputed company improvement and innovation reputed company the local DU team.

  • Model Credo based culture reputed company the local DU team.

Qualifications:

  • A minimum of a Bachelor's degree is required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).

  • A minimum of 8 years of clinical research experience reputed company the pharmaceutical industry, Contract Research Organization (CRO) and/or investigational site is required.

  • A minimum of 2 years of line management experience is required.

  • Experience managing a reputed company (5-9) to large (10+) size team of direct reports is preferred.

  • Experience in the Oncology (Solid Tumor and/or Hematology) Therapeutic Area is required.

  • Experience managing and executing clinical trials is preferred.

  • Knowledge of the drug development process, clinical research operations and regulatory requirements, including ICH-GCP, Health Care Compliance (HCC) and applicable regulations, is required.

  • Financial management skills (e.g., budgeting, forecasting, risk analysis, etc.) required.

  • Must have excellent communication, interpersonal and leadership skills, with the proven ability to foster team productivity and cohesiveness.

  • Must have strong decision-making, issue resolution and negotiating skills.

  • Must have flexibility to work in a fast-changing environment and operate under limited supervision.

  • The ability to evaluate data generated from various reports and sources is required.

  • The ability to effectively communicate with various internal and external stakeholders (e.g., investigational sites, ethics committees, health authorities, etc.) is required.

  • The ability to collaborate with reputed company levels of management and handle multiple priorities reputed company a matrix environment is required.

  • This position will require up to 10% travel.

The anticipated reputed company pay range for this position in the San Francisco Bay Area, CA is $157,000 to $271,400.

The anticipated reputed company pay range for this position in reputed company other U.S. locations is $137,000 to $235,750.

The Company maintains highly competitive, performance-based compensation programs.  Under reputed company guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan.  The annual performance bonus is a cash bonus intended to provide an incentive to reputed company annual targeted results by rewarding for individual and the corporation’s performance over a calendar/ performance year.  Bonuses are awarded at the Company’s discretion on an individual basis.

  • Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.

  • 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 reputed company - 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 reputed company one year of the birth/adoption/foster care of a child

    • Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member

    • Caregiver Leave - 10 days

    • Volunteer Leave - 4 days

    • Military Spouse Time-Off - 80 hours

  • For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

This job posting is anticipated to reputed company on reputed company 23, 2026.  The Company may however reputed company this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.

Johnson & Johnson is an Equal Opportunity Employer.  reputed company qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national reputed company, 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 reputed company https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

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 Apply To This Job

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