Senior Director improving healthcare quality ratings and provider performance for Community Health Plan of Washington. Overseeing strategic initiatives focused on Medicaid and regulatory compliance.
About the role
- Associate Director in Clinical Trial Supply Management at BioNTech, leading global strategies for clinical trials in healthcare innovation.
Responsibilities
- Lead Global Clinical Supply Strategies for global clinical trials
- Ensure patients receive therapies on time
- Develop and oversee distribution, manufacturing, and supply planning strategies
- Manage performance objectives for trials
- Ensure platform portfolio requirements across all clinical trials
- Liaise with interfaces to address trial escalations
- Provide guidance during trial setup, execution, and closeout phases
- Train new team members and ensure adherence to standards
- Ensure compliance with GCP and GMP principles
- Build and maintain relationships with internal and external stakeholders
Requirements
- A relevant university degree in Pharmacy, Chemistry, Biotechnology, Biochemistry, or a related discipline
- Doctorate preferred, if applicable
- At least 5 years of experience in Clinical Trial Supply Management within the pharmaceutical or biotech industry
- Proven track record in managing multiple trial platforms and portfolios
- Developing platform portfolio strategies for clinical trials
- Deep knowledge of GCP and GMP principles, including SOPs, documentation, and ethical standards
- Proficiency in IRT systems and standard office software (e.g., MS Office)
- Extensive knowledge of performance management in IMPM and Quality Management Systems
- Ability to lead individuals with diverse professional backgrounds and expertise levels
- Strong decision-making skills, strategic thinking, and negotiation abilities
- Business-professional English language proficiency.
Benefits
- Competitive remuneration packages
- Health insurance
- Paid time off
- Professional development opportunities
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