Clinical Research Associate/coordinator I

621

Boston, MA, USA
Base: $20.16 - $29.01phly; bonus/equity: not speci...
Hybrid
Patient enrollment in clinical trials
Data entry and source documentation verification
Adverse event monitoring and reporting
The position involves enrolling eligible patients into multiple cancer studies while managing all aspects of data collection and submission

Job Summary

  • The position involves enrolling eligible patients into multiple cancer studies while managing all aspects of data collection and submission.
  • The role serves as a liaison between the clinical team, sponsor, and Institutional Review Board to ensure appropriate communication and reporting.
  • Candidates will be trained on institutional and federal regulations governing clinical research and must maintain strict protocol compliance.

Matching Summary

The position involves enrolling eligible patients into multiple cancer studies while managing all aspects of data collection and submission.

Salary

Base: $20.16 - $29.01/Hourly; Bonus/Equity: Not specified; Benefits: Comprehensive benefits, career advancement, differentials, premiums, and bonuses offered

Skills & Requirements

Must-have

  • Patient enrollment in clinical trials
  • Data entry and source documentation verification
  • Adverse event monitoring and reporting
  • Protocol compliance and regulatory adherence
  • Coordination with IRB and study sponsors

Nice-to-have

  • Experience with electronic medical record review
  • Ability to work independently under supervision
  • Strong analytical and problem-solving skills
  • Effective communication with clinical teams

Key Requirements

  • Bachelor's Degree in related field required
  • 1-2 years of clinical research or compliance experience preferred
  • No degree substitution allowed

Work Rights

Not specified

Tailored Resume

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