8 results
Direct clinical development of zugocaptagene-geleucel for autoimmune disease. Responsibilities include early- and late-stage trial strategy, protocol design, medical monitoring, interpretation of safety and efficacy data, and mentoring clinical development leads. The director also contributes to regulatory submissions and scientific presentations. Based in…
Provide medical oversight for early clinical studies of Tessera’s Gene Writing therapies for hematologic disease. Work includes reviewing eligibility, safety findings and clinical laboratory data, advising investigators, contributing to study designs and interpreting efficacy and biomarker results. The role supports development in indications such as sickle…
Manage global clinical studies for Tessera’s genetic medicine programmes, from trial planning through close-out. Responsibilities include site and vendor selection, study budgets, recruitment planning, clinical documentation and review of trial data quality. The associate director leads cross-functional study teams and works with investigators and external…
Guide Prime Editing programmes from preclinical research into human studies. The medical director develops trial strategies and protocols, monitors participant safety and clinical data, and works with research colleagues on translational biomarkers. Responsibilities also include investigator engagement, regulatory discussions and scientific presentations.…
Lead the medical and clinical development strategy for Beam’s metabolic disease franchise. The role shapes clinical plans and study protocols for base editing therapies, oversees ongoing trials and patient safety, and coordinates clinical and regulatory strategy. Responsibilities include mentoring physicians and clinical scientists and working with research…
Provide scientific and operational pharmacovigilance support for Beam’s therapeutic portfolio. Responsibilities span review of individual and cumulative safety data, signal assessment, risk management, aggregate safety reports and collaboration with clinical development teams. The director also oversees safety vendors and contributes to clinical and…
Support clinical development of gene and base editing therapies through pharmacokinetic, pharmacodynamic and quantitative systems models. The role connects nonclinical and clinical analyses to study design, regulatory documents and programme decisions, and helps develop the clinical pharmacology function. It can emphasise pharmacometrics or combine…
Lead clinical pharmacology and pharmacometric strategy for rare-disease and oncology programmes. Responsibilities include modelling and simulation, Phase 1–3 study design, regulatory documentation and health-authority interactions, working with clinical, translational and preclinical teams.
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