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Enigma Search

Senior Clinical Trial Manager at Enigma Search

Enigma Search No longer available

JOB DESCRIPTION

Senior Clinical Trial Manager

South San Francisco, California, United States

Role Summary

Hands-on clinical trial leader responsible for day-to-day execution of mid to late-stage CKD studies. This role partners closely with cross-functional teams and external vendors to ensure studies are delivered on time, within budget, and with high data quality and compliance standards.

Core Responsibilities

Study Execution

  • Co-lead Phase 2-3 CKD study execution from protocol development through CSR
  • Support key milestones including FPI, enrollment completion, interim analysis, and database lock
  • Lead feasibility assessments and support site selection strategy
  • Develop enrollment forecasts and support KOL engagement with Clinical Science

CRO, Vendor & Site Management

  • Lead RFP process and vendor selection for CROs and trial partners
  • Support contract and budget negotiations
  • Provide day-to-day oversight of CROs, vendors, and sites to ensure performance and compliance

Budget Oversight

  • Track study budgets and manage vendor spend in partnership with Clinical Operations leadership

Quality & Compliance

  • Ensure data integrity and adherence to protocols, SOPs, and ICH-GCP
  • Support inspection readiness efforts with Quality Assurance

Operations & Systems

  • Help evaluate and implement clinical systems (eTMF, CTMS, RBM, etc.)
  • Contribute to SOP development and scalable operational processes

Cross-Functional Collaboration

  • Partner with CMC and Clinical Supply Chain to manage drug supply logistics
  • Work closely with internal functions to ensure smooth study delivery

Qualifications

Required

  • Bachelors degree in scientific or health-related field
  • 58 years Clinical Operations experience, including 4+ years as a CTM
  • Hands-on management of Phase IIIII clinical trials
  • Knowledge of FDA, EMA, and ICH-GCP guidelines
  • Experience with clinical systems (e.g., Medidata Rave, Veeva)
  • Experience with study start-up through close-out
  • CRO/vendor oversight and clinical trial budget tracking experience
  • Strong execution and cross-functional coordination skills
  • Comfortable in fast-paced, growth-stage environment
  • Excellent communication skills
  • Willingness to travel up to ~30%

Preferred

  • Global trial experience
  • Experience in common disease drug development