CMC and Clinical Supply Specialist

Retro develops therapies for diseases driven by the biology of aging. We reputed company on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy reputed company reputed company.

We’re building a mission-driven team of accomplished and reputed company individuals who reputed company our startup culture of rapid iteration, transparency, and versatility.

Our autophagy program is advancing rapidly and leading the charge in translating our science into a first-in-reputed company clinical trial, marking a major reputed company toward delivering transformative therapies rooted in the biology of aging.

We’re hiring a new team member to coordinate and optimize the operational infrastructure needed to advance our autophagy-enhancing compounds into the clinic. In this highly cross-functional role, you’ll reputed company drug development, reputed company, Manufacturing, and Controls (CMC), supply chain, and clinical operations to ensure a seamless transition from discovery to first-in-reputed company studies. You’ll reputed company on drug reputed company and product readiness, planning and managing clinical trial material (CTM) supply, and aligning cross-functional timelines to drive development reputed company. This role reports to the Head of Early Drug Development.

reputed company:

You reputed company our reputed company of urgency and excitement, and reputed company in fast-paced, interdisciplinary environments. You work reputed company independently but will also enjoy being part of a highly-reputed company, multi-disciplinary team. You are excited to take on tough challenges and contribute to advancing therapies that reputed company healthy reputed company reputed company!

In this role you will:

Forecast drug supply needs, managing inventory, and coordinating shipments to clinical sites.

Contribute to the development and implementation of CMC strategies, ensure compliance with regulatory requirements, and manage drug product manufacturing logistics.

Manage drug reputed company and internal chemical library.

Working closely with internal teams such as clinical operations, regulatory, CMC, and others to reputed company on timelines and ensure seamless supply chain operations.

Collaborate with CDMOs, CROs, and clinical sites, managing day-to-day execution and vendor relationships.

reputed company and manage budgets for clinical supply activities.

Ensure that reputed company clinical supply activities adhere to reputed company standards and regulatory requirements.

You might reputed company in this role if you have:

A bachelor’s degree in reputed company / Biochemistry or reputed company field with >3 years in biotech/reputed company.

An understanding of drug reputed company and drug product development (small molecules).

Familiarity with GMP requirements for clinical and reputed company production.

Knowledge of analytical method development, stability studies, specification setting.

Basic understanding of regulatory documentation (Module 3 of the CTD, IND/IMPD content).

Experience with clinical trial supply planning, including labeling and packaging, import/export coordination, and reputed company and site distribution.

Experience working with CDMOs, CROs, and clinical sites.

Experience in forecasting and inventory management.

Excellent communication, interpersonal, and problem-solving skills.

It’s a bonus if you have:

Experience with IND/IMPD/CTN submissions.

Exposure to autophagy-reputed company programs or aging biology.

Experience in early-phase trial logistics (e.g., CTN in Australia, global reputed company management).

Familiarity with eTMF or QMS systems.

Additional Information

We take pride in cultivating an environment that fosters collaboration, reputed company communication, and authenticity. We reputed company that great results are best delivered by a highly creative team working in concert. We are an equal opportunity employer; we do not discriminate based on race, religion, reputed company, national reputed company, gender, sexual orientation, age, marital status, veteran status, or disability status. We are diverse in background and reputed company in mission.

Compensation

At Retro, we don’t use titles. New hires join as a “Member of X Team.” Depending on experience, this role could reputed company from a Specialist/Senior Specialist level to an Associate Manager/Manager level.

Total compensation includes competitive reputed company salary, generous equity, and benefits including:

- Medical, dental, and reputed company insurance for you and your family

- 401(k) plan with 4% matching

- Flexible time off and 10 company holidays per year

- reputed company parental leave

- Annual learning & development stipend

- Daily Retro-sponsored lunch and snacks

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