Added
23 minutes ago
Type
Full time
Salary
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πŸ“‹ Description

  • Contribute to clinical strategy and the development of clinical development plans.
  • Translate scientific and medical objectives into operationally feasible clinical trial designs.
  • Identify clinical development risks and proactively develop appropriate mitigation strategies.
  • Lead or support the development of study protocols, amendments, informed consent documents, case
  • Support site feasibility assessments and investigator selection activities.
  • Provide scientific oversight throughout study startup, enrollment, study conduct, database lock

🎯 Requirements

  • Advanced degree such as PharmD, PhD, OD, MS, MPH, or a related scientific, life sciences, or
  • Candidates with a bachelor's degree and 10+ years of relevant clinical research or clinical
  • Required experience supporting late-stage Phase 2/3 clinical programs and leading the scientific
  • Experience in ophthalmology is preferred.
  • Familiarity with clinical study startup, data cleaning, database lock, closeout, and inspection
  • Strong working knowledge of ICH-GCP guidelines and clinical trial processes.

🎁 Benefits

  • Annual salary range of $158,000–$188,000.
  • Fully remote position within the United States for candidates in eligible states.
  • Comprehensive health insurance coverage for employees and their families.
  • 401(k) matching.
  • Employee Assistance Program (EAP).
  • Flexible Spending Account (FSA).
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