People Matter

Associate Director, Clinical Science

EGenesis

EGenesis

Cambridge, MA, USA
Posted 6+ months ago
COMPANY MISSION
eGenesis is dedicated to giving patients with organ failure a second chance at life by harnessing the power of genome engineering to create safe, effective, and readily available solutions.
POSITION SUMMARY
eGenesis is seeking a highly motivated and experienced Associate Director of Clinical Science to join our Clinical Development team to play a key role in operationalizing eGenesis’ clinical programs across the pipeline. The Clinical Scientist will work cross-functionally with Clinical Operations, Regulatory, Pre-Clinical and Translational to execute study protocols and collect robust and interpretable data throughout the programs.

PRIMARY RESPONSIBILITIES

  • Support the execution of the Phase 1 EGEN-5784 Liver clinical trial, ensuring adherence to regulatory and scientific standards
  • Be a key contributor to protocol development in the EGEN-2784 Kidney program
  • Collaborate with Clinical Operations to optimize the protocol and study-related documents, site selection, enrollment, and ensure protocol adherence and data integrity in all clinical programs
  • Work with internal stakeholders including Clinical Development, Regulatory Affairs, Non-Clinical, and Translational teams to support study strategy and execution
  • Contribute to addressing scientific and procedural questions from sites related to data collection and assessments in the clinical trials
  • Interact with vendors conducting specialized testing or assays; ensure execution aligns with protocol and data quality requirements
  • Serve as the first-level reviewer of clinical data to ensure completeness, interpretability, and alignment with study endpoints, identifying gaps or inconsistencies and work cross-functionally to resolve them
  • Integrate and align data from external labs, registries, and other sources for comprehensive analysis
  • Prepare clinical data summaries for internal and external presentation, and contribute to regulatory submissions
  • Support development of responses to regulatory agencies as part of cross-functional submission teams

BASIC QUALIFICATIONS

  • Ph.D., PharmD, RN, Master's degree with 5+ years of experience in clinical research or drug development in a biotech setting
  • Solid understanding of clinical trial design, data collection standards, and GCP guidelines
  • Strong analytical skills with the ability to analyze and compile complex clinical data
  • Strong experience working with vendors and clinical sites
  • Excellent communication and collaboration skills with both internal teams and external partners