Clinical Trial Supplies Manager

Join to apply for the Clinical Trial Supplies Manager role at Syneos Health Be among the first 25 applicants. The position provides customer-focused leadership of operational and financial aspects of clinical trial supplies management during the complete project life cycle. Duties include liaising with customers, vendors, and investigative sites to manage clinical trial supplies deliverables. Work Here Matters Everywhere We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We continuously build the company we all want to work for and our customers want to work with, creating a place where everyone feels they belong. Job Responsibilities Leadership and Delivery Manages clinical trial supplies for assigned studies and ensures compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), SOPs and regulatory requirements. Accountable for the operational delivery and financial performance of services assigned to the Clinical Supplies team. Liaises with the Supply Chain Logistics Coordinator for IoR/EoR services as required. Leads the identification of and contracting with approved Clinical Trial Supplies vendors, as necessary. Provides vendor management, ensuring key deliverables are met and financial parameters of contracts are upheld. Defines supplies requirements in collaboration with client packaging and distribution vendors and the Project Lead. Oversees the creation, implementation and maintenance of drug and supply distribution plans. Reporting and Communication Accountable for maintenance of project information on a variety of databases and systems. Oversees inventory, supply, and re-supply plans for subject kits and/or study medication required for the duration of a study and provides relevant reports for customers and management. Provides oversight for development and implementation of project plans in accordance with Controlled Documents and ensures proper archival of records in Trial Master Files to ensure inspection readiness. Develops contingency planning and risk mitigation strategies to ensure successful provision of all required clinical trial supplies. Business Development Participates in bid defense meetings to demonstrate overall capabilities of the Clinical Trial Supplies Management team and specific strategies for management of clinical trial supplies logistics for new business opportunities. Develops strong relationships with current and potential customers to ensure satisfaction and identify new business opportunities. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health: syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks or duties at its discretion. Equivalent experience, skills, and/or education are also considered. The Company is committed to compliance with the Americans with Disabilities Act and provides reasonable accommodations when appropriate. This description complies with all applicable legislation. Summary The position provides customer-focused leadership of operational and financial aspects of clinical trial supplies management during the complete project life cycle. Duties include liaising with customers, vendors, and investigative sites to manage clinical trial supplies deliverables. Assignments may range in size and complexity from single service studies to full scope, multiple protocol projects and/or global projects across various phases and functional areas. Seniority level Entry level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr