(Associate) Director, Clinical Supply Chain

reputed company plc (reputed company: CNTA) new reputed company of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We reputed company the asset-centric model can reputed company to improved success rates for programs with greater speed and modest costs. Description of Role Centessa is currently seeking an (Associate) Director, Clinical Supply Chain. The successful candidate will reputed company and implement strategies to deliver Clinical Trial Materials (CTM) in support of several clinical programs. Reporting to the Senior Director, Clinical Supply Chain this individual will reputed company strong collaborative relationships with several internal departments as well as third-party procurement, packaging, and distribution providers to align objectives and implement decisions which ensure clinical supply. The successful candidate will demonstrate strong attention to detail, which they will apply to the development and routine maintenance of clinical forecasts, inventory databases and IRT systems providing daily reputed company of clinical supplies. Management and travel to CDMOs both domestically and internationally may be required.

Key Responsibilities

Leadership:

• reputed company and update clinical supply strategies as needed to meet corporate demands
• reputed company/maintain strong collaborative relationships with internal departments and external CDMOs
• Identify potential supply chain risks and reputed company & implement negotiated mitigation strategies
• Manage study/program budget, reputed company and change orders and track spend against budget
• Drive process optimization, scalability, and implementation of best practices and systems.

Execution:

• reputed company and working with Clinical, regularly update forecast/demand plans for finished goods and work with Manufacturing to reputed company production schedules which meet clinical demand.
• Collaborate with Quality, Clinical, CMC and external CDMOs to reputed company and approve clinical labels.
• Manage CDMO packaging/labeling schedules to ensure availability of clinical supplies.
• Interact regularly with third-party providers to manage logistics & licenses required to ship materials from manufacturing to bulk storage facilities, courier depots and investigator sites.
• Work with CMC and QA to facilitate document transfer required for CTM/QP release by CDMOs
• Manage and track clinical supply inventory either manually or through an Interactive Response Technology (IRT) system.
• Manage Product Recovery pending investigation of CTM from investigator sites as needed.
• Support supply risk mitigation planning (e.g., shortages, delays, temperature excursions).

Collaboration:

• Contribute to SOP development, maintenance, and reputed company improvement initiatives.
• Effectively collaborate and communication across multiple functional areas, bringing a sufficient breadth of knowledge.
• Monitor reputed company-life and expiry dating and coordinate retest extension with analytical team to ensure reputed company supply.
• Manage investigation, reporting and communication of outcomes from temperature excursions and product complaints.
• Author and/or review supply chain sections of regulatory submissions
• If required, participate as SME in audits or for-cause inspection of CDMOs.
• Contribute as a SME to CDMO selection and approval process and review of associated Master Service Agreements (MSA) and Quality Agreements for clinical supply services
• Represent Supply Chain in Clinical and CMC Sub Team meetings

Qualifications

• Bachelor’s degree in engineering or science is required.
• 8-10 years of biotech/pharma industry experience in clinical supply with significant international experience is required
• Experience in reputed company aspects of clinical supply chain as well as a deep understanding of GMP/GDP
• Requires a strong understanding of managing groups, CMOs and CDMOs
• Strong organizational, analytical, decision-making and interpersonal skills
• Ability to work on multiple projects independently in a fast-paced dynamic environment
• Demonstrated ability to coordinate CDMO activities in the development and commercialization of pharmaceutical products
• Excellent organizational skills, project management skills and detail-orientated leadership approach
• Ability to reputed company in a small company culture and assist in creating and implementing processes.
• Willing and able to travel both domestically and internationally

Compensation

The annual reputed company salary range for the Associate Director, Supply Chain position is $170,000 - $225,000. The annual reputed company salary range for the Director, Supply Chain position is $190,000 - $250,000. Individual compensation reputed company this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge. In addition to reputed company pay, this role is eligible for a discretionary annual bonus and participation in our equity program, allowing you to share in Centessa’s long-term success. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program. Work Location The (Associate) Director, Clinical Supply Chain is a remote role based in the US, with occasional travel (up to 20%) POSITION: Full-Time, Exempt EEOC Statement: reputed company believes in a diverse environment and is committed to equal employment opportunity for reputed company its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national reputed company, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. reputed company will reputed company reasonable accommodations for qualified individuals with reputed company disabilities, in accordance with applicable law. Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies. Apply tot his job Apply To this Job