Associate Director, Clinical Supply Remote, United States

We are taking genetic medicine to new heights and into new disease areas to overcome challenges not addressed by existing medicines. This incredible challenge drives our relentless and talented team. Our people are the essence of our inspiring, innovative and collaborative environment that encourages individual contributions and provides opportunities for career development. Living Our Guiding Principles Our company is centered on our guiding principles. They direct every facet of our work, culture, hiring and drive to scale our world‑class genetic medicines company. 4DMT champions diversity, equity and inclusion every single day. Our employee‑led Diversity efforts are inspired by our guiding principles to focus awareness on social equity and create positive change not only within 4DMT, but in our community at large. We also seek to embrace our patient populations so we can help raise awareness. We have had great success in our community partnering with charitable organizations. Current Partners What We Offer We are focused on hiring, inspiring and supporting the best people in the industry who identify with our vision. We create an exciting, dynamic and collaborative environment that fosters dedication to visionary science and medicine, recognizes performance, offers generous benefits and provides challenging opportunities for career development. Join us in creating the future of genetic medicine. Important: Candidates must be authorized to work in the United States and provide valid work authorization documentation throughout their employment in accordance with U.S. immigration requirements. 4DMT welcomes candidates who require nonimmigrant visa transfers or extensions; however, the company does not sponsor new nonimmigrant visa status petitions. 4DMT is a leading late‑stage biotechnology company advancing durable and disease‑targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi‑year sustained delivery of anti‑VEGF (aflibercept and anti‑VEGF‑C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age‑related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery.

GENERAL SUMMARY:

The Associate Director, Clinical Supply is responsible for projecting, planning, executing, and overseeing all supply chain activities related to clinical trial materials. This includes managing the procurement, production, packaging, labeling, distribution, and inventory of clinical trial materials to meet company goals within the defined timelines. This role ensures that clinical supplies, including investigational product, comparators, auxiliary IMPs, and supplies, are delivered on time, within budget, and in compliance with regulatory requirements. This role involves close collaboration with various departments, including Clinical Operations, Clinical Science, Quality Assurance, Regulatory Affairs, Manufacturing, and external vendors. Effective communication with stakeholders at all levels is required to provide regular updates on supply chain status and address any concerns. Serve as the primary point of contact for clinical supply‑related inquiries and issues.

RESPONSIBILITIES:

Supply Planning and Management: Develop and implement clinical supply strategies to support global clinical trials Lead Phase 1 to 3 clinical trial materials planning and execution. Participate in cross‑functional discussions early in the study design phase to ensure that material lead‑time is properly built in for overall program timeline. This includes Investigational Products (IP), diluent, comparator drugs, ancillary supplies, or any other clinical materials required and identified by each project team Create detailed supply plans based on trial requirements, enrollment forecasts, and study timelines Oversee material requirements for domestic and international study execution. Ensure procurement, production, packaging, labeling, and distribution of clinical trial materials are done per applicable local and international guidance Inventory Control and Distribution: Manage inventory levels to ensure sufficient supply of clinical trial materials while minimizing waste. Review clinical supply requests, place ancillary supply orders, and communicate IP demands Coordinate the distribution of clinical supplies to CMO and study sites, ensuring timely delivery and adherence to protocols. Monitor and track shipment status, resolving any issues that arise during transit. Identify, select, and manage relationships with suppliers, manufacturers, and logistics providers including CMOs and CROs. Plan and coordinate clinical supply activities including labeling, packaging, distribution of clinical trial supplies, randomization, and drug accountability systems control. Negotiate contracts and service agreements with vendors to ensure cost‑effective and high‑quality supply chain operations. Project Management: Participate in supply chain business process development projects. Drive continuous operational performance improvement efforts. Ensure compliance with Good Manufacturing Practices and applicable state and federal regulatory authorities. Others Generate and maintain various clinical supply inventory reports. Ensure process execution is conducted per internal policy and procedures. Identify opportunities for process improvements and implement best practices in clinical supply chain management. Perform other duties as assigned.

QUALIFICATIONS:

Education: Bachelor’s degree in supply chain or other disciplines with equivalent industry experience Experience: 8+ years of experience in clinical or in combination with commercial supply chain management, with at least 3 years in a senior or managerial role. In‑depth knowledge of clinical trial processes, GMP, GCP, and regulatory requirements. Proven experience in managing complex global supply chains for clinical trials (including Europe, APAC and South America). Proven experience with high‑complexity Phase 3 trials. Skills: Strong project management skills, with the ability to lead cross‑functional teams and manage multiple priorities. Excellent negotiation, communication, and interpersonal skills. Proficiency in supply chain management software and tools. Strong analytical and problem‑solving abilities. Ability to work in a fast‑paced, dynamic environment and adapt to changing priorities. Travel: Physical Requirements and Working Conditions: Physical Activity – Repetitive motions, making substantial movements of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word. Physical Requirements – Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met. Working Conditions – The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work). Base salary compensation range: $177,000 – $205,000 Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills and years of experience. 4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws. Equal Opportunity Employer / Protected Veterans / Individuals with Disabilities #J-18808-Ljbffr 4D Molecular Therapeutics, Inc.