Associate Director, Clinical Supply Project Manager - Program (Hybrid)

Remote Full-time
Welcome to Merck & Co, a global healthcare company with a mission to improve the lives of patients around the world. We are seeking a highly motivated and experienced Associate Director, Clinical Supply Project Manager - Program to join our team. In this role, you will have the opportunity to work on innovative projects that will have a direct impact on patient care. We are looking for a dynamic and driven individual with strong project management skills and a background in clinical supply chain management. If you are passionate about making a difference in the pharmaceutical industry and meet the required qualifications, we encourage you to apply for this exciting opportunity.

Oversee and manage all aspects of clinical supply chain management for assigned projects.
Collaborate with cross-functional teams, including clinical operations, logistics, quality, and regulatory, to ensure timely and efficient delivery of clinical supplies.
Develop and maintain project timelines, budgets, and risk management plans.
Coordinate and communicate with external vendors and partners to ensure timely and accurate delivery of clinical supplies.
Monitor and track inventory levels to ensure adequate supply for ongoing and upcoming clinical trials.
Proactively identify and address potential supply chain issues and implement solutions to mitigate risks.
Work closely with clinical operations to forecast demand and plan for future supply needs.
Lead and participate in regular project team meetings to provide updates on clinical supply status and address any issues or concerns.
Manage and track project expenses and provide regular budget updates to management.
Stay current with industry developments and best practices in clinical supply chain management to continuously improve processes and procedures.
Mentor and provide guidance to junior project management team members.
Represent the company in a professional manner and maintain strong relationships with internal and external stakeholders.
Adhere to company policies, procedures, and regulatory guidelines.
Ensure compliance with all applicable laws, regulations, and standards related to clinical supply chain management.
Foster a positive and collaborative work environment to promote team success and individual growth.

Merck & Co. is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

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