Associate Director, Clinical Development Program Management
Lyell Immunopharma
This senior leadership position manages clinical development programs from early through late-stage trials, serving as the central accountability point for cross-functional program delivery. The role requires translating clinical strategy into operational plans, coordinating with core teams and external partners to ensure trials progress on schedule and within budget while maintaining regulatory compliance.
Responsibilities
- Lead strategic and operational execution of clinical development programs from early to late-stage
- Serve as central accountability point for cross-functional program delivery and milestone achievement
- Drive alignment on scope, timelines, budget, and risk across multiple functional teams
- Identify obstacles and develop mitigation strategies in partnership with program leadership
- Support regulatory submissions including IND and BLA/NDA documents
Requirements
- Proven track record leading complex matrixed teams through clinical trials to approval
- Deep understanding of clinical development process and regulatory pathway
- Experience with GCP compliance and applicable regulatory requirements
- Ability to translate clinical strategy into operational plans and manage risk
- Cross-functional collaboration skills across Clinical, CMC, Regulatory, and Finance
$190k - $230k
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...Associate Director, Clinical Scientist Vir Biotechnology, Inc. is a clinical-... ...-stage portfolio includes programs for chronic hepatitis delta... ...Medical Monitoring, Data Management, Biostatistics, and Regulatory... ...programs from early development through key clinical milestones...Full timeWork at officeWork visa3 days per week- ...Description Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial... ...to participate in our long-term incentive programs. Note: No amount of pay is considered to...Full timeLocal area
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