Added
22 minutes ago
Type
Full time
Salary
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risk management project management clinical research clinical trial management ich guidelines

πŸ“‹ Description

  • Provide direction and operational expertise for all Clinical Site Management (CSM) integrity
  • Influence and align within Clinical Development Operations, with other assigned Site Management
  • Analyze study timelines and overall study assumptions to confirm deliverables are feasible for CSM.
  • Accountable for study level site monitoring strategy, documented in Site Monitoring Plan.
  • Ensure study-level and/or area-level timelines are maintained across the study lifecycle.
  • Drive site-level activities at study level and/or area level, including site selection, activation

🎯 Requirements

  • Bachelor's Degree or equivalent OUS degree, typically in (para)medical or scientific field.
  • A minimum of 5 years+ of industry clinical research experience including 2 years of monitoring or
  • Preferred exposure in study initiation through study completion in multiple phases of studies
  • Experience in multiple therapeutic areas or disease state/indications highly desired.
  • Demonstrates a high level of core and technical competencies through management of various
  • Possesses good communication skills and demonstrated leadership abilities, able to influence

🎁 Benefits

  • Medical/Dental/Vision insurance
  • 401(k) retirement plan
  • Paid time off (vacation, holidays, sick)
  • Eligible to participate in long-term incentive programs
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