Added
13 days ago
Type
Full time
Salary
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Related skills

project management data collection clinical research statistical analysis regulatory compliance

πŸ“‹ Description

  • Lead the planning, execution, monitoring, and completion of assigned clinical research projects
  • Coordinate cross-functional project teams to ensure activities comply with applicable regulations
  • Oversee project operations, budgets, regulatory requirements, and patient safety
  • Manage essential clinical study documents (protocols, SOPs, informed consent forms, case report
  • Assign and track interdisciplinary activities including site monitoring, database development, data
  • Serve as primary point of contact for sponsors and clients, managing expectations and resolving

🎯 Requirements

  • Bachelor's degree in Health Sciences, Clinical Research, or related field
  • 1-3 years of experience in clinical study management
  • Strong understanding of clinical research processes and regulatory requirements
  • Excellent project management and organizational skills
  • Strong written and verbal communication skills
  • Ability to build collaborative working relationships

🎁 Benefits

  • Education Reimbursement program for full-time employees
  • Monthly Cell Phone and Remote Work Allowance
  • One-time office setup allowance
  • Working while visiting program – up to 4 weeks per year
  • Flexible Summer Hours Program from May – September
  • Employee referral incentive
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