Clinical Research Manager

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Upper East Side, New York, US
$106,350.00 - $125,350.00 py
On-site
Clinical trial oversight
Protocol compliance
Adverse event reporting
Contributes to the management and oversight of clinical trials, coordinating activities related to clinical studies, monitoring and documenting progress

Job Summary

  • Contributes to the management and oversight of clinical trials, coordinating activities related to clinical studies, monitoring and documenting progress.
  • Participates in the oversight and monitoring of investigator/coordinator compliance with IRB and institutional requirements and the approved protocol.
  • Serves as liaison between site personnel and the sponsor, and performs PFTs as a back for research subjects.

Matching Summary

Contributes to the management and oversight of clinical trials, coordinating activities related to clinical studies, monitoring and documenting progress.

Salary

$106,350.00 - $125,350.00

Skills & Requirements

Must-have

  • clinical trial oversight
  • protocol compliance
  • adverse event reporting
  • ICH/GCP guidelines
  • regulatory document maintenance

Nice-to-have

  • strong analytical skills
  • attention to detail
  • self-motivated
  • works with minimal supervision

Key Requirements

  • Bachelor's Degree in Life Sciences
  • Minimum five years on-site monitoring experience
  • Experience with FDA Audit preferred
  • CCRP and/or CCRA certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter