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Iambic Therapeutics, a clinical-stage AI-driven drug discovery company founded in 2020, is seeking an Associate Medical Director or Medical Director to join its Clinical Development team. The role focuses on study execution and oversight of a Phase 1 clinical oncology program, with additional support for pipeline programs preparing for IND submission.
Key responsibilities include serving as medical monitor for assigned clinical trials, providing medical and scientific expertise throughout the study lifecycle. You will work cross-functionally with clinical operations, regulatory sciences, data management, biostatistics, clinical pharmacology, and nonclinical teams to ensure high standards of study conduct. Safety oversight is critical: you will review adverse events, serious adverse events, and protocol deviations, collaborating with pharmacovigilance to assess safety signals. Additional duties include guiding patient eligibility and protocol adherence, preparing study-related documents (protocols, Investigator Brochures, informed consent forms, clinical study reports), reviewing and interpreting clinical trial data, supporting regulatory agency interactions, establishing partnerships with key opinion leaders and patient advocacy organizations, developing advisory board content, and preparing abstracts, presentations, and manuscripts for publication.
The company is based in San Diego with a state-of-the-art facility featuring onsite gym and dining. The role offers industry-leading competitive pay, company-paid healthcare, flexible spending accounts, voluntary life insurance, 401K matching, and uncapped vacation.
QUALIFICATIONS:
- MD or PharmD with clinical oncology experience and biotech/pharma oncology drug development experience preferred; alternatively, PhD with minimum 3 years of biotech or pharmaceutical experience in oncology drug development
- Experience as a medical monitor on a clinical trial, including patient eligibility review, site interaction for protocol adherence oversight, protocol deviation review, clinical data review and cleaning, and coding
- Experience executing clinical studies and interacting with regulatory agencies
- Excellent written and verbal communication skills
- Ability to work effectively in cross-functional teams with internal and external partners
- Strong organizational and time management skills with attention to detail and proven ability to handle multiple tasks efficiently
- Creative problem-solving skills and proactive approach
