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Program Transformation Associate Director
Pharmaceutical Product Development (PPD)
Remote, North Carolina, United States of America
Work Schedule
Environmental Conditions
Job Description
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.
Asa 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:
- Equivalent experience in the field will be considered in lieu of a Bachelor of Science degree, with preference given to candidates holding an advanced degree.
- 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
Thermo Fisher Scientific Inc. is proud to be an equal opportunity employer, committed to creating a diverse and inclusive workplace. We value and celebrate individuals with different experiences, backgrounds, and perspectives. We strive to provide equal employment opportunities for all qualified individuals. As an equal opportunity employer, we are also dedicated to providing reasonable accommodations for applicants with disabilities during the job application process. If you require any accommodations, please contact us at 1-855-471-2255. We look forward to hearing from you and considering you for this exciting opportunity.
Apply today at http://jobs.thermofisher.com and #StartYourStory with Thermo Fisher Scientific Inc.
Job posted: 2024-05-31
