Associate Director, Program Management Leader

jj; Beerse; Hybride; EUR 96 000 - 165 000; Plein temps

Résumé du poste

Johnson & Johnson Innovative Medicine in Beerse, Belgium, is recruiting for a senior Associate Director, Program Management Leader in a hybrid role. You will translate the CDT strategy into a Compound Development Plan and lead the PMT to ensure execution and governance across the CDT and cross-functional partners.

The role requires extensive PM experience in pharmaceutical R&D, strong leadership, and ability to navigate complex global drug development; travel up to 20% may be required.

Qualifications

• A minimum of a Bachelor’s degree is required, preferably in a Life Science (Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
• A minimum of 8 years in Pharmaceutical, CRO or a related Healthcare industry is required.
• Experience in and knowledge of the pharmaceutical development process is required.
• Experience in Project Management within Research & Development is required.
• Knowledge of Project Management systems, methodologies and tools required.
• Project Management Certification (PMP, CPM, etc.) is preferred.
• Clinical research operational knowledge is required.
• Experience across early and late phases of studies (Phase I-IV) is preferred.
• Experience in the Oncology therapeutic area is preferred.
• Experience mentoring/coaching others is preferred.
• Must have excellent communication and presentation skills.
• Must have exceptional interpersonal skills, including the ability to persuade, negotiate, and moderate conflict.
• Must have strong leadership skills and proven ability to foster team productivity and cohesiveness.
• Must have strong decision-making, analytical and strong financial management skills.
• The ability to manage all aspects of execution of a clinical trial is required.
• The ability to lead without authority and in muti-functional matrixed and global environments.
• This position will require up to 20% domestic and international travel.

Responsabilités

• Enable the CDT to deliver program outcomes by establishing, monitoring and refining program scope, timelines, and budget with cross-functional partners.
• Apply PM methodologies, R&D knowledge to build scenarios, validate assumptions, assess resource needs, provide cost estimates, and surface risks.
• Translate the CDT strategy into a Compound Development Plan.
• Navigate the CDT through drug development complexity to obtain strategy approval and resources.
• Lead and manage the PMT sub team of the CDT, uniting project managers across functions to implement the program execution plan.
• Create, maintain, and communicate the cross-functional risk-management register.
• Ensure the program stays on track financially and on schedule by managing changes and mitigation actions.
• Cultivate and monitor a high-performing team environment across CDT and cross-functional teams, with clear accountabilities.

Connaissances

Budgeting

Clinical Trial Designs

Clinical Trials

Compliance Management

Consulting

Contract Management

Execution Focus

Fact-Based Decision Making

Give Feedback

Industry Analysis

Laboratory Operations

Organizing

Process Improvements

Project Integration Management

Research and Development

Research Ethics

Technical Credibility

Formation

Bachelor’s degree in Life Science (Biology, Chemistry, Biochemistry, Nursing, Pharmacy)

Advanced degree preferred

Description du poste

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Beerse, Antwerp, Belgium

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 https://www.jnj.com/innovative-medicine

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):

• United States - Requisition Number: R-095458
• Belgium - Requisition Number: R-099566

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

Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Program Management Leader. This position is a hybrid role and will be located in Beerse, Belgium.

The Associate Director, Manager, Program Management Leader (PML) will be responsible for translating the Compound Development Team (CDT) strategy into a Compound Development Plan (CDP). The PML will lead the Program Management Team (PMT) and ensure the operationalization of the CDP.

Principal Responsibilities:

• Enable the CDT to deliver program outcomes by establishing, monitoring and continuously refining program scope, timelines, and budget in collaboration with all cross-functional partners.
• Apply PM methodologies, R&D and organizational knowledge to build scenarios, validate assumptions, assess resource requirements, provide cost estimates, and surface operational risk and mitigation strategies for governance review.
• Translate the CDT strategy into a Compound Development Plan.
• Navigate the CDT through the complexities of the drug development process and the Johnson & Johnson Innovative Medicine environment to obtain strategy approval and secure vital resources.
• Lead and manage the PMT sub team of the CDT, bringing together all project managers across the functions to establish, integrate, implement, monitor, and adapt the program execution plan.
• Create, maintain, and communicate the cross-functional risk-management register.
• Ensure the program stays on track financially and according to schedule by identifying changes and monitoring impacts, managing changes, and actively driving issue mitigation.
• Cultivate and monitor a high-performing team environment in the CDT and across the cross-functional program “Team of Teams” by creating a trusted and learning environment and establishing and monitoring teaming principles and practices, including clear accountabilities and decision rights, meeting rhythms and communication & escalation pathways.

Additional Responsibilities may include the following:

• Early Therapeutic Area Leader (ETAL):
  • Serve on the TA Discovery Portfolio Council (DPC) to operationalize early portfolio strategy in close partnership with TA discovery and Discovery, Product Development and Supply (DPDS) leadership.
  • Serve as the decision support leader.
  • Optimize discovery processes and business rules to ensure high-quality reporting and cross- therapeutic area (cross-TA) consistency.
• Disease Area Stronghold (DAS)/Pathway Area Stronghold (PAS) PML:
  • Coordinate all activities to establish and the DAS/PAS strategy, aligned with TA and organization objectives.
  • Contribute to and coordinate portfolio strategy updates over time, including the DAS/PAS Reviews.
  • Manage and communicate DAS/PAS strategic and operational guidance to core and extended DAS/PAS teams, governance, and portfolio reporting.
  • Cultivate and monitor a high-performing DAS/PAS team environment.
• Licensing and Acquisition (L&A) PML:
  • Apply PM methodologies, R&D and organizational knowledge to build scenarios, validate assumptions, assess resource requirements, provide cost estimates, and surface operational risk and mitigation strategies for governance review throughout the Due Diligence team engagement until final deal terms.
  • Transition knowledge to the CDT once the deal is signed and the asset is brought into the portfolio.

Qualifications:

• A minimum of a Bachelor’s degree is required, preferably in a Life Science (Biology, Chemistry, Biochemistry, Nursing, Pharmacy). Advanced degree preferred.
• A minimum of 8 years in Pharmaceutical, CRO or a related Healthcare industry is required.
• Experience in and knowledge of the pharmaceutical development process is required.
• Experience in Project Management within Research & Development is required.
• Knowledge of Project Management systems, methodologies and tools required.
• Project Management Certification (PMP, CPM, etc.) is preferred.
• Clinical research operational knowledge is required.
• Experience across early and late phases of studies (Phase I-IV) is preferred.
• Experience in the Oncology therapeutic area is preferred.
• Experience mentoring/coaching others is preferred.
• Must have excellent communication and presentation skills.
• Must have exceptional interpersonal skills, including the ability to persuade, negotiate, and moderate conflict.
• Must have strong leadership skills and proven ability to foster team productivity and cohesiveness.
• Must have strong decision-making, analytical and strong financial management skills.
• The ability to manage all aspects of execution of a clinical trial is required.
• The ability to lead without authority and in muti-functional matrixed and global environments.
• This position will require up to 20% domestic and international travel.

#LI-Hybrid

Required Skills:

Budgeting, Clinical Trial Designs, Clinical Trials, Compliance Management, Consulting, Contract Management, Execution Focus, Fact-Based Decision Making, Give Feedback, Industry Analysis, Laboratory Operations, Organizing, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Technical Credibility

Preferred Skills:

Budgeting, Clinical Trial Designs, Clinical Trials, Compliance Management, Consulting, Contract Management, Execution Focus, Fact-Based Decision Making, Give Feedback, Industry Analysis, Laboratory Operations, Organizing, Process Improvements, Project Integration Management, Research and Development, Research Ethics, Technical Credibility

The anticipated base pay range for this position is:

€96,000.00 - €165,025.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees' and companies' performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some locations eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.