What are the responsibilities and job description for the Clinical Operations Lead position at Talently?
Job Title: Clinical Operations Lead
Location: On Site - San Diego, California, United States
Salary: $125000-$150000
Skills: Clinical Trial Management, GCP Compliance, Vendor Collaboration, Precision Medicine, Study Documentation
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.
Salary : $125,000 - $150,000