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You will lead the development and qualification of innovative bioanalytical assays to support immunogenicity risk assessments, biomarker measurements, and clinical pharmacology deliverables for genetic medicines. You will work cross-functionally to inform key program decisions and contribute to a portfolio of targeted therapies.

You'll lead global Phase 1-3 clinical trial execution for a late-stage biotech's lung portfolio, providing strategic and operational leadership. Your impact will ensure **inspection-ready compliance** and **timely delivery** of programs advancing durable genetic medicines.

You'll **ensure compliance** of 4DMT's quality document and records management system, supporting **GxP regulations** and inspection readiness in a hybrid role at our Emeryville office. You'll drive process improvements and **perform operational tasks** across document lifecycles for a late-stage biotech company.

You'll lead the planning and delivery of clinical and regulatory documents for a gene therapy in late-stage development. Your core impact will be ensuring BLA readiness for 4D-150, a potential backbone therapy for retinal vascular diseases. This role stands out due to its central role in a critical regulatory submission for a novel genetic medicine.

You'll provide **Tier 1/2 IT Helpdesk support** for lab equipment and applications in a biotech environment. Your work will ensure **data integrity and regulatory compliance** for GMP systems. You'll collaborate across teams to support **validation and operational activities**.

You'll lead a team of translational scientists and drug development experts bringing innovative gene therapies to patients. Your core impact will be setting strategy for translational products and overseeing preclinical studies from concept through Phase 2. This role offers the chance to shape the future of gene therapy at a leading late-stage biotechnology company.

You'll provide **Quality Assurance oversight** for global clinical trials, ensuring compliance with **GCP regulations**. You'll develop quality plans, manage audits, and support inspection readiness at a **leading late-stage biotech company**.

You'll support day-to-day execution of a **Phase 3 clinical trial**, including start-up, conduct, and close-out activities. You'll serve as key liaison between sponsor, clinical sites, and CRO partners for **unmasked clinical operations**. This contract role offers **remote work** within the US.

You will own the strategy, delivery, and operational integrity of information systems supporting clinical research and development. You will ensure clinical systems are fit for purpose, inspection-ready, and maintained in a validated state while advancing technology solutions for efficient clinical execution.

You will manage day-to-day operations of phase 1-3 clinical trials, including start-up, conduct, and close-out activities. This role involves overseeing CROs and service providers, leading cross-functional teams, and ensuring compliance with GCP and regulatory requirements.