Associate Director Clinical OperationsMeet Life Sciences • San Francisco, CA, United States
Associate Director Clinical Operations
Meet Life Sciences • San Francisco, CA, United States
[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]12+ years of progressive clinical operations experience within the biotech or pharmaceutical industry Must have prior experience functioning at the Associate Director level or equivalent, as this is a high-visibility leadership role with significant oversight responsibilities. Demonstrated success overseeing global Phase 1–3 clinical trials Strong candidates from any therapeutic area will be considered Extensive vendor and CRO management expertise Ability to operate effectively in a fast-paced, dynamic environment Excellent leadership, communication, and problem-solving skills Ability to be on-site in the Bay Area on a hybrid schedule Mid-Senior level Full-time Project Management, Research, and Science Biotechnology Research and Pharmaceutical Manufacturing
This range is provided by Meet Life Sciences. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$190,000.00 / yr - $225,000.00 / yr
Additional compensation types
Annual Bonus and Stock options
Associate Director, Clinical Operations
Location : Hybrid, Bay Area
Start Date : December 2024 or January 2025
Our client, a fast-moving biotechnology company, is urgently hiring an Associate Director of Clinical Operations to lead global programs across Phases 1–3. This individual will oversee complex clinical trials within neurology / CNS, though candidates from all therapeutic areas will be considered if they bring strong global oversight experience at the AD level.
Key Responsibilities
- Provide strategic and operational leadership for global clinical studies across Phases 1–3
- Manage study timelines, budgets, vendors, CROs, and cross-functional execution
- Ensure adherence to ICH / GCP, protocol requirements, and internal quality standards
- Lead risk mitigation efforts, resolve operational issues, and maintain data quality
- Partner closely with Clinical Development, Regulatory, Biometrics, and external partners
- Represent Clinical Operations in governance meetings and program-level discussions
- Mentor and guide team members supporting assigned programs
Qualifications
If you meet these qualifications and are available to start in December or January, we’d welcome a conversation. Referrals are also appreciated.
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