Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research 64 Non-MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
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.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.
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
Johnson & Johnson Innovative Medicine is recruiting for a Senior Director, Compound Development Team Leader (CDTL). The CDTL provides leadership to a cross-functional strategic compound development team and leads the development and execution of the compound strategy. Further, the CDTL champions the product/brand at all levels of J&J and is responsible for managing the alignment on communication on all CDT matters, as appropriate.
Key Responsibilities
Actively contributes to Compound Strategy decision-making by ensuring relevant research, analysis, and expertise is available.
Leads CDT in partnership with line functions to successfully develop the compound such that its value is maximized over its lifecycle while costs and time are minimized without sacrificing quality.
Builds team effectiveness, and leads the Compound Development Team (CDT) to achieve its goals through the networks of people/functions represented on the team. When necessary, negotiates with function heads on functional deliverables.
Challenges all functions on CDT to ensure that all issues and questions are being addressed, and that line function input into strategy and plans is adequate to meet the needs of the compound.
Leads the development and maintenance of the compound development strategy in collaboration with the Project Manager (PM).
Identifies potential issues and leads contingency planning; leads CDT problem solving and applies decision-making tools and techniques. Drives CDT to make effective and efficient decisions.
Leads resolution of conflict at the CDT, Oncology Senior Leadership Team (Oncology SLT), Development Committee (DC), Investment Committee (IC), Group Operating Committee (GOC) and joint steering committees for partnered compounds and senior management levels.
Ensures successful implementation of clinical supplies strategy.
Accountable for overall budget and project plan deliverables.
Acts as co-chair of global project teams with Alliance partners and aligns global strategy within a partnership, as applicable.
Major collaborator for the internal Alliance Managers for partnered compounds.
Ensures lessons learned at critical nodes in the development path.
Leads the communication of strategy, issues, and plans to the PMC, Oncology SLT, DC, IC, GOC, alliance partners, JPKK, regional management boards, and other key stakeholders.
Represents the interests of the compound/brand along with the global commercial lead at the Oncology SLT.
Builds and maintains team effectiveness and satisfaction.
Drives innovation by benchmarking
Works with functional management to:
1. Secure the required resources for project success
2. Influence optimal team composition
3. Align goals and objectives with CDT members
4. Coach and guide CDT members
5. Provide input for performance evaluation of CDT members
Goal: Align and implement on the Oncology SLT strategy.
General Requirements:
Candidate is preferred to hold a PhD, MD or M.D./Ph.D with minimum of 8-10 years, Masters with 10-12 years or equivalent experience in a leadership role as a part of a research-driven pharmaceutical company. Experience in leading clinical development programs in the appropriate TA is preferred.
Qualified candidates will have demonstrated a solid understanding of and involvement in the entire drug development process. He or she should have proven ability to work cross-functionally with interdisciplinary teams to access and optimize resources for development programs and experience working in a matrix organization. Candidate should be business orientated, having managed resources and budgets with proven record of leading projects trough successful transition from Discovery to Early Development and advancement of projects through preclinical and clinical development to Phase 2b within the therapeutic area. Excellent communication and leadership skills are a must, and a strong track record of producing results in a matrix-based environment is essential.
Domestic and international travel may be required of approximately 10 - 25% (depending on the compound type and stage of development).
This is a role that should be filled by a high performing individual in the organization who demonstrates outstanding leadership, influence, and communication skills.
Strong problem solving skills for developing creative solutions and meeting project objectives is required. Strong project planning and tracking skills. Demonstrated ability for strategic thinking and contingency planning.
Expert knowledge of the drug development process and familiarity with pharmaceutical portfolio risk management is required. Must understand requirements for successful commercialization of a new product.
Expert interpersonal skills for bridging between scientific and business participants, for negotiating timelines, resources and for effective international collaborations. Expert oral/written communication skills, allowing effective interactions with all levels of the organization. Expert critical and objectives interpretation of scientific and commercial information. Expert analytical skills for integrating and interpreting interdisciplinary project information.
High degree of organizational awareness and understanding of change management.
Required Skills:
Global Drug Development, Oncology Drug Development, Pharmaceutical Development
Preferred Skills:
Clinical Evaluations, Clinical Trial Protocols, Consulting, Cross-Functional Collaboration, Design Mindset, Drug Discovery Development, Entrepreneurship, Good Clinical Practice (GCP), Lateral Leadership, Medicines and Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific Research, Strategic Change, Study Management
The anticipated base pay range for this position is :
$196,000.00 - $342,700.00
Additional Description for Pay Transparency:
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 60 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado 68 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 60 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
