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8 hours ago
Type
Full time
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πŸ“‹ Description

  • Accountable for driving study level global and/or area level CSM deliverables by targeted timelines
  • Analyze study timelines and overall study assumptions to confirm deliverables are feasible for CSM.
  • Ensure study-level and/or area-level timelines are maintained across the study lifecycle. Provide
  • Oversee monitoring activities at study and/or area level in collaboration with other assigned SMLs
  • Proactively identify, evaluate, and mitigate risks, ensuring effective action plans; key
  • Collaborate with other assigned SMLs and stakeholders in the Clinical Study Team to address and

🎯 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 year of monitoring or
  • Preferred exposure in study initiation through study completion in multiple phases of studies
  • Demonstrates a high level of core and technical competencies through management of various
  • Possesses good communication skills and demonstrated leadership abilities. Able to influence
  • Competent in application of standard business procedures (Standard Operating Procedures

🎁 Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance
  • 401(k) to eligible employees
  • Eligibility to participate in long-term incentive programs
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