Job description
Mantell Associates is partnered with one of the most exciting CROs who are experiencing high levels of growth and expansion across Europe and US. They are seeking a highly motivated and experienced Global Head Clinical Trial Supply.
As the Global Head Clinical Trial Supply, you will be responsible for overseeing and managing the clinical trial supply chain for all ongoing clinical trials worldwide. You will collaborate with various internal and external stakeholders to ensure the timely delivery of high-quality clinical trial supplies that meet the regulatory and quality requirements.
Key Responsibilities:
Lead and manage the clinical trial supply chain for all clinical trials globally
Develop and implement clinical supply strategies that align with the company's goals and objectives
Collaborate with cross-functional teams to ensure that the clinical trial supply chain is integrated into the overall clinical trial plan
Develop and manage budgets, timelines, and resources to ensure that clinical trial supplies are delivered on time and within budget
Ensure that all clinical trial supplies are produced, packaged, labeled, shipped, and stored in compliance with regulatory requirements and quality standards
Manage relationships with external vendors, including contract manufacturing organizations, clinical supply depots, and logistics providers
Provide technical expertise to internal and external stakeholders on clinical trial supply chain topics, including packaging and labeling, import/export regulations, and cold chain management
Ensure that appropriate risk management strategies are in place for clinical trial supply chain activities
Stay up-to-date with industry trends and best practices related to clinical trial supply chain management
Qualifications:
Bachelor's degree in pharmacy, chemistry, or a related field. A master's degree or PhD is preferred
Minimum of 10 years of experience in clinical supply chain management in the pharmaceutical or biotech industry
In-depth knowledge of clinical trial supply chain processes, including packaging and labeling, import/export regulations, and cold chain management
Strong understanding of global regulatory requirements related to clinical trial supply chain management
Experience managing relationships with external vendors, including contract manufacturing organizations, clinical supply depots, and logistics providers
Excellent communication, collaboration, and leadership skills
Strong analytical and problem-solving skills
Ability to work effectively in a fast-paced, dynamic environment
Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information get in contact with Megan Field on +44 203 3854 7700 or megan.field@mantellassociates.com if you're looking to take a step up in your career.