JOB SUMMARY
The Senior Clinical Trial Manager, Clinical Operations, serves as the operational lead for assigned early-phase oncology studies, providing end-to-end trial leadership from start-up through close-out. In close partnership with Clinical Development, Regulatory, Biometrics, and external CROs, this role drives high-quality, inspection-ready trial execution within a collaborative, growth-stage biotech environment. The Senior CTM is accountable for vendor oversight, risk management, timeline and budget performance, and cross-functional alignment to ensure studies are delivered efficiently and in compliance with global regulatory requirements, with primary responsibility for international regions, including Europe, Asia-Pacific, and United Kingdom, and secondary oversight of North America. This position reports to the Director of Clinical Operations and is remote in the EU or UK.
KEY RESPONSIBILITIES
- Provide end-to-end operational leadership for complex, multi-regional clinical trials from start-up through close-out, ensuring delivery on time, within budget, and in compliance with global regulations and company SOPs
- Lead cross-functional study teams and drive alignment across Clinical Development, Regulatory, Biometrics, and external partners
- Develop and execute enrollment, site management, and monitoring strategies to ensure high-quality trial conduct and performance
- Oversee CRO and vendor performance, including KPI management, monitoring quality oversight, document review and approval, and vendor selection support
- Partner with Data Management and Medical to conduct ongoing data review and ensure timely query resolution
- Develop and manage key study documents and operational tools, including protocols, informed consent forms, project plans, budgets, and study materials.
- Lead study-related training for investigators, site personnel, and internal teams.
- Proactively identify, assess, and escalate operational risks with mitigation strategies and clear recommendations.
- Mentor and support junior clinical operations staff, including potential dotted-line management responsibilities.
- Travel up to 10–20% to support regional study oversight and site engagement
QUALIFICATIONS
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, or related scientific discipline required; with 7+ years of progressive clinical trial management experience in biotech, pharmaceutical, and/or CRO environments
- Demonstrated expertise managing clinical trials from start-up through close-out, with experience overseeing multi-regional, multi-site studies and global CRO partners
- Experience in oncology clinical trials required; solid tumor and early-phase (Phase I/Ib or II) experience preferred
- Strong knowledge of EU Clinical Trial Regulation (EU CTR 536/2014), ICH-GCP (E6 R2/R3), GDPR, and applicable local regulatory requirements across EU member states.
- Experience with clinical trial submissions via CTIS and coordination with Ethics Committees and Competent Authoritie
- Excellent written and verbal communication skills in English; additional EU languages are a plus
- Proficiency with clinical trial systems, including CTMS, eTMF platforms, IRT systems, EDC systems, and safety databases
- Ability to thrive in a collaborative, fast-paced, growth-stage biotech environment with evolving priorities and high accountability
ABOUT IAMBIC THERAPEUTICS
Iambic is a clinical-stage life-science and technology company developing novel medicines using its AI-driven discovery and development platform. Based in San Diego and founded in 2020, Iambic has assembled a world-class team that unites pioneering AI experts and experienced drug hunters. The Iambic platform has demonstrated delivery of new drug candidates to human clinical trials with unprecedented speed and across multiple target classes and mechanisms of action. Iambic is advancing a pipeline of potential best-in-class and first-in-class clinical assets, both internally and in partnership, to address urgent unmet patient need. Learn more about the Iambic team, platform, pipeline, and partnerships at iambic.ai.
MISSION & CORE VALUES
Our mission is to deliver better medicines through innovations in AI-based discovery technologies. The culture and work at Iambic Therapeutics are profoundly strengthened by the diversity of our people and our differences in background, culture, national origin, religion, sexual orientation, and life experiences. We are committed to building an inclusive environment where a diverse group of talented humans work together to discover therapeutics and create technologies.
PAY AND BENEFITS
We offer industry leading competitive pay, company paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation to our team.