Clinical Operations Lead

Talently; San Diego (CA); On-site; USD 100,000 - 150,000; Full time

Job summary

Talently is seeking a Clinical Operations Lead in San Diego, California, to drive clinical trial operations in an innovative biotechnology research organization. The role involves collaboration with teams to execute clinical studies, ensuring compliance with GCP standards and quality requirements.

The ideal candidate has 3–7+ years of clinical operations experience, particularly with Phase I–III trials. Join a team that supports transformative initiatives in longevity science and precision health in a high-growth environment.

Qualifications

• 3–7+ years of experience in clinical operations within biotechnology, pharma, or CRO settings.
• Demonstrated support of Phase I–III clinical trials.
• Deep understanding of Good Clinical Practice (GCP) and clinical trial processes.

Responsibilities

• Support end-to-end clinical trial operations across multiple concurrent studies.
• Collaborate with CROs, sites, and vendors to ensure high-quality study execution.
• Track and report on study timelines, milestones, and key deliverables.

Skills

Clinical operations experience

Phase I–III clinical trials

Good Clinical Practice (GCP)

Project management

Job description

About the Biotechnology Research Company / The Opportunity:

Join a rapidly growing, innovation-driven organization operating at the forefront of biotechnology research, focused on precision health and genomics. This is an opportunity to support transformative clinical initiatives in longevity science and personalized medicine. As Clinical Operations Lead, you will collaborate with talented teams, oversee multiple clinical studies, and gain significant exposure to the latest advances in data‑driven healthcare—all within a high‑growth environment known for strong leadership and robust funding.

Responsibilities:

• Support end-to-end clinical trial operations across multiple concurrent studies.
• Collaborate with CROs, sites, and vendors to ensure high‑quality study execution and performance.
• Track and report on study timelines, milestones, and key deliverables.
• Assist with site selection, initiation, monitoring, and closeout activities in compliance with quality standards.
• Ensure strict adherence to GCP, SOPs, and all applicable regulatory requirements.
• Contribute to the development and maintenance of clinical documentation, including protocols and monitoring plans.
• Partner cross‑functionally with clinical, regulatory, and data teams for seamless program advancement.

Must‑Have Skills:

• 3–7+ years of experience in clinical operations within biotechnology, pharma, or CRO settings.
• Demonstrated support of Phase I–III clinical trials.
• Deep understanding of Good Clinical Practice (GCP) and clinical trial processes.
• Proven ability to manage multiple projects and priorities in a fast‑paced environment.
• Experience collaborating with CROs and external vendors on clinical programs.

Nice‑to‑Have Skills:

• Exposure to genomics, precision medicine, or working with complex clinical datasets.
• Background in oncology or longevity science‑focused programs.
• Strong cross‑functional partnering skills, especially with regulatory and data teams.
• Experience authoring clinical protocols, reports, and monitoring plans.
• Adaptability to growth environments and a passion for innovation in life sciences.