Clinical Supply Chain Manager

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔗 Supply Chain

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Provide customer-focused leadership of operational and financial aspects of clinical trial supplies management throughout the project life cycle • Liaise with customers, vendors, and investigative sites to manage Clinical Trial Supplies deliverables • Manage clinical trial supplies for assigned studies and ensure compliance with GMP, GCP, SOPs, and regulatory requirements • Ensure operational delivery and financial performance of assigned Clinical Supplies services • Liaise with the Supply Chain Logistics Coordinator for IoR/EoR services as required • Identify and contract with approved Clinical Trial Supplies-related vendors • Manage vendors and ensure deliverables and contract financial parameters are met • Define supplies requirements with client packaging and distribution vendors and the Project Lead • Oversee drug and supply distribution plans • Maintain project information in databases and systems • Oversee inventory, supply, and re-supply plans for subject kits and study medication • Provide relevant reports for customers and management • Oversee project plans and archival of records in Trial Master Files • Develop contingency plans and risk mitigation strategies • Participate in bid defense meetings for new business opportunities • Develop relationships with current and potential customers to ensure satisfaction and identify new business opportunities

🎯 Requirements

• Bachelor’s Degree (or equivalent) qualification in Life Sciences, Medicine, Pharmacy, Nursing, or a related field • Equivalent experience, skills, and/or education will also be considered • Prior experience in a contract research organization, pharmaceutical, or biotechnology company in project management or clinical trial supplies management • Strong knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practices, and applicable regulatory requirements • Strong organizational skills • Ability to manage time and work independently • Excellent written and spoken English communication, presentation, and interpersonal skills • Ability to inform, influence, convince, and persuade • Flexibility and ability to handle multiple tasks and meet deadlines while delivering high-quality work in a dynamic environment • High level of competency in English • Proficiency with MS Office Applications • Ability to travel as necessary, up to 25%

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Reasonable accommodations, when appropriate • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Multiple career paths and employment opportunities