What are the responsibilities and job description for the Clinical Supply Chain Project Manager position at Collabera?
Job Summary:
The Clinical Project Manager I will support clinical supply chain operations across Phase I through Phase IV clinical trials. This role is responsible for managing protocol-level supply activities, ensuring timely availability of investigational products, and coordinating cross-functional execution. The position requires strong project management capabilities, regulatory awareness, and the ability to operate effectively in a collaborative clinical development environment.
Key Responsibilities:
• Manage clinical supply chain activities at the protocol level for Phase I through Phase IV clinical trials
• Forecast, plan, schedule, and coordinate supply activities to ensure timely availability of investigational products
• Partner with clinical study teams to influence protocol design and optimize supply chain efficiency
• Translate clinical study designs into packaging and labeling strategies
• Author study medication and labeling sections within clinical protocols
• Develop protocol-specific labeling in compliance with global regulatory requirements
• Track project timelines, milestones, and logistics to ensure successful execution
• Perform scenario analysis, risk management, and contingency planning for clinical supplies
• Forecast bulk drug product requirements, comparator agents, and ancillary supplies
• Ensure adherence to standard operating procedures and regulatory compliance requirements
Required Qualifications:
• Bachelor’s degree in physical science, biological science, engineering, pharmacy, or a related field
• Minimum 2 years of experience in the pharmaceutical industry
• Experience in areas such as drug discovery, drug development, clinical operations, supply chain, or quality assurance
• Strong project management and organizational skills
• Ability to manage multiple priorities and deadlines effectively
• Strong written and verbal communication skills
• Working knowledge of global regulatory standards and compliance practices
Preferred Qualifications:
• Experience in clinical supply chain or clinical project management
• Understanding of clinical development lifecycle and trial execution
• Experience working in cross-functional teams within regulated environments
Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.
Pay Range: $40/hr to $48/hr
Salary : $40 - $48