BioAge Labs (BIOA) is finding new ways to treat disease by targeting the mechanisms of aging, with the ultimate goal of increasing healthy human lifespan. https://bioagelabs.com. Backed by a16z, Pear VC and Felicis.
About the role
The CTA plays a critical role in the execution of Phase 1–3 clinical trials and is responsible for ensuring operational excellence, inspection readiness, and compliance with ICH/GCP guidelines and company SOPs. This position partners closely with Clinical Trial Managers, CROs, vendors, and investigative sites to support timely and high-quality study delivery. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Bachelor’s degree in a scientific or healthcare-related field preferred, equivalent experience considered
- 2-3+ years of clinical operations experience in biotechnology, pharmaceutical, or CRO settings
- Experience supporting Phase 1–3 clinical trials
- Hands-on experience with TMF management and clinical systems (eTMF, CTMS, EDC)
- Working knowledge of ICH/GCP and applicable regulatory requirements
- Strong organizational skills and exceptional attention to detail
More about this role
BioAge Labs (BIOA) is finding new ways to treat disease by targeting the mechanisms of aging, with the ultimate goal of increasing healthy human lifespan. https://bioagelabs.com
BioAge is seeking a Clinical Trial Associate (Senior CTA) to join our Clinical Operations team.
The CTA plays a critical role in the execution of Phase 1–3 clinical trials and is responsible for ensuring operational excellence, inspection readiness, and compliance with ICH/GCP guidelines and company SOPs. This position partners closely with Clinical Trial Managers, CROs, vendors, and investigative sites to support timely and high-quality study delivery.
- Independently support and coordinate clinical trial activities from start-up through close-out.
- Partner with CTMs to ensure operational milestones, timelines, and deliverables are achieved.
- Serve as primary owner of Trial Master File (TMF) quality, completeness, and inspection readiness.
- Perform ongoing TMF quality control and resolve documentation gaps with internal teams and vendors.
- Collaborate with CROs, vendors, and sites to ensure study milestones and deliverables are met.
- Track study timelines, identify risks, and proactively escalate...
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