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Eikon Therapeutics, a biopharmaceutical company founded on Nobel Prize-winning innovations, is seeking a Senior Director of Clinical Research to lead clinical development efforts. The role combines medical expertise with operational oversight of early-stage clinical trials in oncology and non-oncology programs.
As Study Responsible Physician, you will design and conduct clinical development trials, assess safety and efficacy data, perform medical monitoring, and manage study-related clinical activities. You'll interpret research reports, prepare written and oral results, and ensure quality and timeliness of deliverables. The position requires close collaboration with cross-functional teams including discovery scientists, translational researchers, biomarker specialists, toxicologists, clinical pharmacologists, drug safety experts, and regulatory personnel.
Key responsibilities include working with Clinical Science, Data Management, Clinical Operations, and Biostatistics teams to ensure integrated execution and systematic oversight of study protocols. You will address protocol questions from Health Authorities and Ethics Committees in a consistent manner, serving as a key bridge between internal functions and external regulatory bodies.
The role requires a minimum of 3 days per week onsite in the Jersey City office, with flexibility for additional presence as business needs require. This is an opportunity to advance novel therapeutics for patients while working with a team leveraging cutting-edge microscopy technology that enables molecular-resolution measurements of protein movement in living cells—unlocking new classes of drug targets.
Qualifications: MD or DO with significant oncology experience, minimum 5-7 years clinical experience including 3+ years in drug development, and demonstrated expertise in clinical trial design and execution.
