Distribution Project Coordinator

Distribution Project Coordinator Catalent’s Philadelphia, Pennsylvania site serves as the company’s North American Center of Excellence for clinical supply packaging, delivering comprehensive, end‑to‑end support for global clinical trials across multiple therapeutic modalities. The site provides integrated services including direct comparator sourcing, blinding and manufacturing, primary and secondary packaging, storage and distribution, and clinical returns management, enabling efficient and compliant trial execution. It also plays a growing role in supporting biologic as well as cell and gene therapy programs, with enhanced cold‑chain and cryogenic handling capabilities designed to meet the complex requirements of advanced therapies. As a critical hub within Catalent’s global clinical supply network, the Philadelphia site helps sponsors accelerate development timelines while maintaining the highest standards of quality, flexibility, and regulatory compliance. Our Philadelphia site is located in the Bensalem/Northeast Philadelphia area. Position Summary We have an opportunity for a Distribution Project Coordinator to join our team. This role focuses on managing distribution for clinical trial protocols, maintaining strong client relationships, and collaborating closely with project management for study‑specific setup. The position offers the chance to work in a dynamic environment supporting global clinical trials and ensuring timely, compliant distribution operations. Shift: Monday - Friday, 8:00am to 4:30pm Please Note: Start and end times may fluctuate daily to meet business need Location: Philadelphia, PA 100% Onsite The Role Work with Project Management to define study‑specific distribution needs; Anticipate and resolve distribution problems, reporting findings to Project Management and the client Ensure execution aligns with customer expectations and agreed scope of services Manage customer order pipeline, including guiding Sales & Operations Planning teams and Distribution on upcoming orders Coordinate scheduling of international and large‑volume shipments with the Distribution Department Generate and maintain Distribution Master Checklists for shipment protocols with appropriate approvals Ensure study drug shipments comply with all applicable Standard Operating Procedures and customer‑approved protocols Review material setup in enterprise systems for distribution‑specific items All other duties as assigned The Candidate Minimum Requirements Associate degree or equivalent work experience is required; Bachelor’s degree is preferred Strong attention to detail with the ability to manage multiple priorities and meet deadlines in a fast-paced environment. Proficiency in Microsoft Office and the ability to quickly learn ERP and business systems. Effective communication, negotiation, presentation, project management, and relationship-building skills. Ability to work independently, exercise sound judgment, solve problems, and make ethical decisions; Demonstrated initiative, teamwork, continuous improvement mindset, and results-driven execution under pressure. Preferred Requirements At least 1-2 years of customer service experience in a current Good Manufacturing Practice regulated environment is preferred Experience with distribution, cold-chain operations, cGMP, and FDA regulations is preferred Why You Should Join Catalent Defined career path and annual performance review and feedback process Diverse, inclusive culture Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives Competitive paid time off plus 8 paid holidays Community engagement and green initiatives Medical, dental, and vision benefits effective day one of employment Tuition reimbursement Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patien…

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