Program Transformation Associate Director

7 months ago


Swindon, United Kingdom Thermo Fisher Scientific Full time

Thermo Fisher is redefining what it means to support drug development companies, providing best in class services, products, and support to accelerate clinical timelines. Be at the forefront of crafting one-of-a-kind solutions and changing the way we think about and support our customers. These solutions cross the boundaries between groups and divisions and reelevate the way we work together to deliver products and services to the industry.

As a Program Transformation Associate Director, you will focus on developing long-lasting customer relationships based on trust and timely service delivery, helping clients to achieve their goals. You will act as the client advocate across Thermo Fisher’s broad network of services and lead assigned integrated supply & delivery (ISD) program optimization initiatives through start-up, delivery, and closure. You will further govern streamlined communication through cross-functional and cross-business project teams to deliver a successful and outstanding customer experience. This is a cross functional and cross group offering inclusive of services from our Pharma Services Group (PSG) and Clinical Research Group (CRG).
- Responsibilities:
- Support effective communication pathways / information sharing between Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO) teams including responsibility to clearly define ownership of activities
- Lead process improvement initiatives and pre-award client prioritization workshops
- Consider, develop, and maintain relevant metrics to demonstrate improvements in quality and reduction in risks and issues
- Define ownership of activities and provide study-specific guidance
- Support leadership meetings with updates on progress, challenges, and solutions
- Triage integrated business queries and support resolution of integrated business issues
- Coordinate financial aspects of assigned activities
- Requirements:
- Minimum 5-8 years relevant industry experience in project and/or functional management in Pharmaceutical, Biotech, CRO, CDMO, and/or Clinical Supply/Supply Chain management
- Certification in Project Management methodologies preferred
- Deep understanding of drug product development, clinical supply management, and clinical project delivery
- Excellent communication and presentation skills
- Proficiency in data analysis and visualization tools
- Ability to motivate and influence without direct authority
- Strong planning ability, capable to develop and implement clear and detailed strategies in support of process optimization
- Familiarity with Good Manufacturing Practices and Good Clinical Practices
- Ability to travel as assignments require
- Explore Location



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