CDD - Human Trials Manager (F/H/NB)

Ensure Roll-out and training as needed of Human Trials procedure across the site. Key Tasks: Coordination of Human Trials Supplies Lead the Coordination Efforts: Establish required documentation with 3rd parties and establish or assist in writing manufacturing & labelling instructions for internal operations. Collaborate with Cross-Functional Teams: Work closely with R&D, clinical operations, and other relevant departments to gather trial requirements and ensure seamless supply chain operations. Evaluate Current SOPs: Conduct a comprehensive review of existing Human Trials Supply SOPs and identify areas for improvement to enhance efficiency and simplify processes. Support implementation: Lead the rollout and support training for the new Human Trials Supply SOP, ensuring all team members are trained and compliant. Education: Bachelor's degree in Life Sciences, Supply Chain Management, or a related field. Advanced degree preferred. Experience: Minimum of 5 years of experience in Human Trials supply, clinical trial management, or a related field, preferably within the pharmaceutical or healthcare industry. Skills: Strong project management and organisational skills. Excellent communication and interpersonal skills. Familiarity with regulatory requirements related to human trials and/or cosmetic regulations. Proficiency in English essential

Global life science company with pharmaceuticals, consumer health, and crop science divisions. Headquartered in Leverkusen, Germany.

bayer.com