via Indeed
$70K - 90K a year
Manage end-to-end supply chain for clinical trials ensuring timely distribution and inventory optimization.
Requires 5+ years project management experience in clinical research/clinical trial supplies environment with strong communication and leadership skills.
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as Project Manager Clinical Supplies - To manage the end-to-end supply chain for clinical trials, ensure timely and efficient distribution of trial materials, maintain optimal inventory levels, and collaborate with cross-functional teams to support the successful execution of clinical studies. This is a full-time, fully remote position. Candidates must be located in the United States, specifically Eastern Time Zone (ET). Project management experience in a CRO/clinical research/clinical trial supplies environment is a requirement. Essential Functions: • Develop study specific plans for each assigned project. • Meet with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets. • Integrate all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements. • Participate in ongoing training on new regulations. • Representing the department internally and externally at meetings, strategic projects and initiatives as per the business requirements. • Mentor and guide support junior team members. • Participate in process improvement initiatives. • Maintain and use existing tools while continuously looking for improvement opportunities. • May participate in the bidding and/or bid defense opportunities client contact for their supply chain requests/questions/concerns. Education and Experience: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). Project management experience in a clinical research/clinical trial supplies environment is a must. In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Strong English and communication skills both written and verbal • Strong interpersonal, planning, organizational, problem solving, sense of urgency and decision-making skills • Effective leadership and team building skills • Strong working knowledge of Microsoft Office suite • Strong focus on customers and attention to detail • Ability to work in team environment, as well as work independently with little guidance • Good understanding of clinical supply operations • Solid client building and 3rd party relationship management • Ability to provide customer service with the highest standards of quality and excellence Working Conditions and Environment: • Work may be performed in a production, office or home-based environment with exposure to electrical office equipment. • Occasionally travels both domestic and international Physical Requirements: • Frequently stationary for 6-8 hours per day. • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. • Frequent mobility required. • Occasional crouching, stooping, bending and twisting of upper body and neck. • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. • Ability to access and use a variety of computer software developed both in-house and off-the-shelf. • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. • Frequently interacts with others to obtain or relate information to diverse groups. • Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration. • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. • Regular and consistent attendance. Salary Transparency This is a salaried role that will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. Compensation will be initially discussed during the screening period, with actual compensation confirmed in writing at the time of offer. We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally include: • A choice of national medical and dental plans, and a national vision plan • A wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Accounts (HSAs) or Health Savings Account (HSA) • Tax-advantaged savings and spending accounts and commuter benefits • Employee assistance programs • At least 120 hours paid time off (PTO). 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer rime off in accordance with company policy. • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthrough.
This job posting was last updated on 5/26/2026