Senior / Executive Medical Director, Clinical Development (Oncology)
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Before you apply
SalaryNo pay range posted
LocationSan Diego HQ
Work modeon-site
Typefull-time
SeniorityDirector
Experience5+ yrs
DepartmentClinical
Company size201–500 people
PostedAug 7, 2026 · 3mo ago
Verified live3h ago
May no longer be actively hiring
Posted by the company on Aug 7, 2026No pay range listed, though California requires one
At a glanceSummarised by Seekless from the posting.
M.D. or D.O. (or international equivalent); board eligibility/certification in hematology/oncology or medical oncology strongly preferred
Meaningful drug-development experience in biotech or pharma
5+ years for a Senior Medical Director and 8–10+ years for an Executive Medical Director
Direct, hands-on experience authoring and executing IND submissions
Direct experience designing and running Phase 1 / early-phase oncology clinical trials
Demonstrated experience with oncology assets and a strong understanding of the oncology therapeutic and drug-development landscape
Working knowledge of GCP, ICH guidelines, and the global regulatory environment for oncology development
Experience with small-molecule oncology programs and targeted therapies
Experience taking a program from candidate nomination or IND through clinical proof-of-concept
Comfort working in a fast-paced, data-rich, technology-forward environment and collaborating with computational and platform teams
Prior experience presenting to health authorities and/or supporting BD due diligence
Benefits
Health insurance
401(k)
Flexible time off
About the role
JOB SUMMARY
We are seeking a Senior or Executive Medical Director to provide medical and clinical development leadership for our early-stage oncology portfolio. This individual will own the clinical strategy and execution for one or more assets from IND-enabling activities through first-in-human and early efficacy studies. You will serve as the clinical and scientific lead on cross-functional program teams, working closely with our discovery, translational, regulatory, and clinical operations groups — and directly alongside our AI/ML platform teams — to translate novel candidates into well-designed clinical programs.
This position will be based in our San Diego Headquarters.
Title and scope will be calibrated to the successful candidate’s experience.
Responsibilities
KEY RESPONSIBILITIES
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Serve as the clinical/medical lead for early-stage oncology programs, owning the clinical development strategy from IND through Phase 1 and early proof-of-concept.
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Author and drive the clinical components of IND submissions, including protocols, investigator’s brochures, and clinical sections of regulatory documents; support and participate in health authority interactions (e.g., pre-IND, EOP1).
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Design first-in-human and early-phase oncology trials, including dose-escalation and dose-optimization strategies, biomarker and translational plans, and eligibility criteria.
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Provide ongoing medical monitoring and safety oversight for active trials, including review of emerging safety data, dose decisions, and management of study conduct in partnership with Clinical Operations and Pharmacovigilance.
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Partner with translational science and the AI/ML platform teams to define patient selection strategies, pharmacodynamic endpoints, and data-driven development hypotheses.
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Engage key opinion leaders, investigators, and study sites; represent programs to internal governance, partners, and, as appropriate, external stakeholders.
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Collaborate cross-functionally with Regulatory Affairs, CMC, Clinical Operations, Biostatistics, and Program Management to keep programs on strategy and on timeline.
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Contribute to portfolio-level decisions, candidate selection input, and business development / due diligence as needed.
Requirements
QUALIFICATIONS
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M.D. or D.O. (or international equivalent); board eligibility/certification in hematology/oncology or medical oncology strongly preferred; exceptional candidates with PharmD and relevant oncology and clinical experience will be considered
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Meaningful drug-development experience in biotech or pharma. We anticipate roughly 5+ years for a Senior Medical Director and 8–10+ years for an Executive Medical Director; strong candidates across this range are encouraged to apply.
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Direct, hands-on experience authoring and executing IND submissions.
•
Direct experience designing and running Phase 1 / early-phase oncology clinical trials.
•
Demonstrated experience with oncology assets and a strong understanding of the oncology therapeutic and drug-development landscape.
•
Working knowledge of GCP, ICH guidelines, and the global regulatory environment for oncology development.
Nice to have
PREFERRED QUALIFICATIONS
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Experience with small-molecule oncology programs and targeted therapies.
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Experience taking a program from candidate nomination or IND through clinical proof-of-concept.
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Comfort working in a fast-paced, data-rich, technology-forward environment and collaborating with computational and platform teams.
•
Prior experience presenting to health authorities and/or supporting BD due diligence
About the company
ABOUT IAMBIC THERAPEUTICS
Iambic Therapeutics (Nasdaq: IAM) is a technology and clinical-stage life sciences company headquartered in San Diego. By utilizing molecular superintelligence — integrating proprietary AI with automated, scalable chemistry and biology experimentation — our platform is designed to address the totality of drug discovery and development. At Iambic, we are building an engine that is designed to power the future of medicine. Learn more at iambic.ai.
MISSION & VALUES
Our mission is to make better technology for better medicines. Three values guide how we work:
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Bold. We are courageous, take thoughtful risks, and approach challenges with tenacity.
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Innovative. We are creative and find new solutions that deliver impact.
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Collaborative. We respect one another and partner with integrity.
We value the range of perspectives our people bring, and we work to build an environment where every team member can contribute and grow.
Benefits
PAY AND BENEFITS
The pay range for this role is listed above. Actual pay depends on factors including experience, skills, and location. Eligible employees in the U.S. receive company-paid medical coverage, flexible spending accounts, voluntary life insurance, 401(k) matching and flexible time off. We are in a brand-new state-of-the art facility in beautiful San Diego with a community gym, dining, and easy access to great places to live and play.
Legal
EQUAL OPPORTUNITY
Iambic is an equal opportunity employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, ancestry, age, disability, medical condition, genetic information, marital status, veteran or military status, or any other characteristic protected by law.