Senior Director, Compound Development Team Leader-...
Role details
Job location
Tech stack
Job description
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Matrix Leader of Cross-functional Compound Development Team; Works with TA Leadership Team to develop compound strategy
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Leads the development and maintenance of the program plan and decision-making by providing relevant research, analysis, and expertise
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Manages successful cross-functional execution of the project plan through negotiating with Function heads about functional deliverables
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Aligns the CDT to achieve its goals through the networks of people/functions represented on the team
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Identifies critical risks and assumptions and transparently communicate them to the CDT, functions, TA & Pharma governance committees, and senior management
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Identifies issues and leads contingency planning
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Leads resolution of issues at the CDT, TA & Pharma governance committees and senior management levels
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Leads CDT problem-solving and provide decision-making tools and techniques
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Leads the communication of strategy and plans to the TA & Pharma governance committees, development partners, and other key stakeholders
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Responsible for review of medical publications emerging from the Team and its affiliates
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Accountable for the budget for the compound or program
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Works with Function heads to:
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Select CDT members
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Set Goals and Objectives for CDT members
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Mentor and guide CDT members
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Provide input for performance evaluation of CDT members
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Execute the program and manage deliverables & financials
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May act, in concert with senior clinical personnel, as a company spokesperson regarding publication of clinical research findings and presentations to relevant health authorities (e.g. global health authority meeting related to NDA/MAA/BLA)
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Develop credible relationships with scientific leaders, key regulatory officials
Requirements
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Advanced Degree (Ph.D., M.D., M.B.A.) highly desirable
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A minimum of ten years of pharmaceutical industry or related experience overall and/or a minimum of five to seven years of drug development or related experience
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Experience in a leadership role within a multi-functional R&D organization
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Ability to integrate all cross functional disciplines into a successful strategy and project plan
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Understanding of requirements for successful commercialization of a new product
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Expert knowledge of the drug development process and the competitive environment
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Strong problem solving skills for developing creative solutions and meeting project objectives
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Demonstrated influence, negotiation and conflict resolution skills, including the ability to influence without clear reporting authority
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Significant work experience in a leadership position in a team matrix environment
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Strong planning and tracking skills
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Demonstrated ability of strategic thinking and contingency planning with respect for Johnson & Johnson Innovative Medicine objectives
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Fluent in written and spoken English
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Working knowledge of the use of Microsoft suite of software products including Excel and Word
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Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings
Required Technical Knowledge and Skills:
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Fluent in written and spoken English
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Working knowledge of the use of Microsoft suite of software products including Excel and Word
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Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings
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)
Benefits & conditions
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 Company's consolidated retirement plan (pension) and savings plan (401(k)).
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