Role Summary
Senior Specialist, Clinical Supply Chain in Watertown, MA. Responsible for planning and coordination of end-to-end clinical supply for clinical studies, including forecasting, inventory management, distribution, accountability, and return/destruction. Hybrid work schedule with an on-site role in Watertown.
Responsibilities
- Primary monitor/representative for clinical site inventory management, temperature excursions, distribution, accountability, return and destruction of investigational medicinal product (IMP) for multiple Phase 3 clinical trials.
- Collaborate with cross-functional teams to ensure timely and accurate delivery of clinical supplies to study sites to support site activation and patient dose.
- Monitor global clinical supply inventory at the clinical site level for IXRS/IRT and traditional studies, tracking milestone dates and adjusting the drug distribution plan accordingly.
- Implement supply strategies to de-risk missed patient visits, maximize supply efficiency, and minimize waste.
- Identify and escalate supply chain risks and/or issues.
- Support IXRS/IRT development.
- Monitor and perform tasks within ERP and IXRS/IRT system(s).
- Support management of relationships with external vendors and supplies to ensure timely and cost-effective delivery of supplies.
- Participate in meetings and provide updates on project progress, milestones and potential risks.
- Maintain accurate and organized records of clinical supply chain activities and assist with data analysis as needed.
- Assist with Trial Master File (TMF) setup, maintenance, and closure relating to IP Supplies.
- Prepare standard documents, such as purchase orders or shipping documentation.
- Identify areas for process improvement and make recommendations for increased efficiency and cost reduction.
- Adhere to all company policies and procedures including safety, quality, and cGxP compliance.
- Continuously develop and expand knowledge of clinical supply chain processes.
- Assist with production planning and forecasting.
Qualifications
- Strong communication, problem solving, and time management skills.
- Ability to thrive in a fast-paced environment while remaining flexible, proactive, resourceful, efficient, and detail-oriented.
- Ability to complete tasks within agreed timelines and resources through managers’ guidance.
- Ability to work well with a diverse team from various functions.
- Proficient in Microsoft Applications (Word, Excel, PowerPoint).
- Excellent written and verbal communication skills.
- Attention to detail and ability to prioritize tasks to meet critical deadlines.
- Strong commitment to compliance and ethical standards.
Education
- Associate or Bachelor's degree in supply chain management or science-related field.
Experience
- 2+ years of experience in a Clinical Supply Chain role in a Biotechnology or Pharmaceutical environment, or 4+ years of relevant work experience in a similar field; bachelor’s degree required.
- 2+ years of experience working in a GxP regulated environment.
- Basic understanding of logistics and inventory management.
- Strong planning and organizational skills with flexibility and attention to detail.