About this opportunity
BioPhase lists this Associate Director of Clinical Operations opportunity in san diego, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
We are seeking an experienced clinical operations professional to support the planning and execution of global clinical studies. This role partners cross‑functionally to drive study delivery, ensuring timelines, budgets, and quality standards are met in alignment with regulatory requirements.
Key Responsibilities
Lead day‑to‑day oversight of clinical trials from start‑up through close‑out
Manage CROs and vendors to ensure high‑quality, on‑time study execution
Track study timelines, budgets, and performance metrics; communicate risks and updates to leadership
Ensure compliance with GCP, ICH, and applicable regulatory standards
Contribute to key study documents (protocols, reports, operational plans)
Support vendor selection, study planning activities, and process improvements
Maintain TMF quality and overall study documentation
Mentor junior team members and support a collaborative, accountable team environment
Qualifications
BS/MS in life sciences or related field
7+ years of clinical research experience, including global trial management
Strong background across Phases I–III with CRO/vendor oversight
Solid understanding of GCP/ICH and regulatory requirements
Experience contributing to clinical documentation and study deliverables
Strong communication, organization, and cross‑functional collaboration skills
Comfortable working across time zones with occasional travel (~10%)
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Worksite address
san diego, TX, 78384, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.