Distribution Project Coordinator

About the role

Collaborate with Project Management to define study-specific distribution requirements and shipment strategies. Coordinate, schedule, and dispatch clinical trial materials to sites, including courier bookings and required approvals. Track shipments post-dispatch, proactively address distribution issues, and communicate updates to Project Managers and clients. Coordinate on-site material destruction activities in accordance with study and compliance requirements. Support Quality and Project Management in resolving quality issues, customer complaints, and supplier concerns. Review distribution summaries and generate or maintain Distribution Master Checklists (MCLs) for shipment protocols. Create and manage just-in-time labeling worksheets to support distribution timelines. Set up and manage studies within Interactive Response Technology (IRT) platforms. Prepare and review commercial (proforma) invoices and support invoice processing requirements. Participate in customer meetings, audits, courier discussions, and distribution-related site visits as needed. Other duties as assigned. The Candidate: Bachelor's degree required. Minimum of 5 years of relevant industry experience in a cGMP environment, or comparable pharmaceutical knowledge and experience. JD Edwards or comparable ERP systems preferred. Demonstrate strong analytical skills and problem-solving skills. Strong knowledge of MS Office software and query-based systems activities (e.g., Pivot Tables, VLOOKUP's, Excel Formulas, building presentations in PowerPoint, etc.). Proven written, verbal, and interpersonal communication skills are required. Strong project management and customer service skills are required. Ability to work effectively under pressure to meet competing workplace demands and appropriately prioritize tasks as required. Physical Requirements: Individual needs to be accessible to lab and office staff and able to use required office equipment. Specific vision requirements include reading of written documents and use of computer monitor screen frequently The anticipated salary range for this role in California is $70,000 - $80,000. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why you should join Catalent: Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, on-site yoga classes, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment. Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean-up activities for community engagement. Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives. Several Employee Resource Groups focusing on Diversity and Inclusion. Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment. 152 hours of PTO + 10 paid holidays. Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic. Tuition Reimbursement - Let us help you finish your degree or earn a new one! WellHub program to promote overall physical wellness. Perkspot - offers exclusive or private discounts fro