<p>Clinical Supply Chain Manager</p> <p>Job Description</p> <p>The Clinical Supply Chain Manager will ensure the effective management of drug manufacturing and the clinical supply chain, ensuring seamless provision of drug and ancillary supplies across the clinical portfolio. This role requires collaboration with internal clinical supply chain, clinical operation, regulatory, and manufacturing colleagues to assist in the delivery of clinical supplies in line with regulatory requirements and internal quality processes.</p> <p>Responsibilities</p> <ul> <li>Lead and provide direction around Supply Chain discussions in team meetings, maintaining effective communication with customers and partners. </li><li>Set up the clinical supply chain strategy for studies and/or clinical portfolio of studies. </li><li>Design and implement labeling, packaging, and supply strategies that meet study design, clinical study sites, and regulatory authority requirements, while maximizing supply efficiency. </li><li>Manage, with input from CMC and Regulatory groups, the generation and approval of label texts, translations (where required), and label proof. </li><li>Produce a clinical supply agreement document detailing the design, setup, and operation of the supply chain for responsible studies or groups of studies. </li></ul> <p>Essential Skills</p> <ul> <li>Experience in supply chain management and clinical supplies. </li><li>Knowledge of IRT, Cold Chain, GxP, GmP, and regulatory compliance. </li><li>Vendor management and pharmaceutical forecasting expertise. </li><li>Proficiency in budget management, labeling, and shipping processes. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Degree or higher in a relevant scientific subject or business management, or equivalent industry experience. </li><li>Masters or PhD in a relevant scientific subject is desirable. </li><li>Demonstrated computer skills with a functional knowledge of Microsoft packages (MS Word, Excel, Power Point, Outlook, MS Project, SharePoint). </li></ul> <p>Work Environment</p> <p>This role requires a presence on-site three to four days a week, either in Conshohocken, PA or Gaithersburg, MD. Join a leading T-Cell Oncology biotech company with a strong pipeline, offering opportunities for long-term growth into senior positions.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $140000.00 - $155000.00/yr.</p> <p>Holidays: 9 fixed plus 2 floating</p> <p>Vacation: Up to 20 days/year (5-day carryover)</p> <p>Sick Leave: 10 days/year</p> <p>Workplace Type</p> <p>This is a hybrid position in Conshohocken,PA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Jul 23, 2025.</p> <p>About Actalent</p> <p>Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.</p> <p>The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.</p> <p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>