Clinical Research Associate, Sponsor Dedicated

Lifelancer
Springfield, MA
Job Description
Perform site monitoring visits and manage study data to ensure compliance with study protocol, regulations, and sponsor requirements. Collaborate with study team members and manage site financials. Required: 2 years of on-site monitoring experience, Good Clinical Practice knowledge, therapeutic and protocol knowledge, computer skills, written and verbal communication skills.

Requirements

  • Perform site monitoring visits
  • Manage study data
  • Collaborate with study team members
  • Manage site financials

Benefits

  • Health and welfare benefits
  • Incentive plans
  • Bonuses
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