Clinical Research Associate / Sr Clinical Research Associate

Agilent Technologies, Inc.

$86,456.00 - $135,088.00pyr; bonus, stock + benefi...
**
Gcp, study protocol, procedures adherence
Site initiation and close-out visits
Source data verification (sdv)
** Agilent Technologies, Inc. is seeking a Clinical Research Associate (CRA) or Senior Clinical Research Associate (Sr CRA) to monitor clinical studies, ensure compliance with regulations, and support site staff. The position is fully remote and offers competitive compensation, along with opportunities for professional growth within a dynamic and inclusive company culture. **

Job Summary

  • Performs all study monitoring visits and completes supporting visit reports, including applicable visits such as site/investigator qualification, site initiation, interim monitoring, remote monitoring, and close-out visits.
  • Assures adherence to GCP, study protocol, procedures, all applicable requirements, and regulations throughout the study monitoring visits.
  • For Senior CRA, demonstrates a high degree of competence in clinical research with prior exposure to all aspects of clinical study and functions at a proficient level of independence with a significant degree of autonomy in conducting clinical research.

Matching Summary

Match Score: 75

** Agilent Technologies, Inc. is seeking a Clinical Research Associate (CRA) or Senior Clinical Research Associate (Sr CRA) to monitor clinical studies, ensure compliance with regulations, and support site staff. The position is fully remote and offers competitive compensation, along with opportunities for professional growth within a dynamic and inclusive company culture. **

Salary

$86,456.00 - $135,088.00/yr; Bonus, stock and benefits eligibility; Not specified

Skills & Requirements

Must-have

  • GCP, study protocol, procedures adherence
  • Site initiation and close-out visits
  • Source Data Verification (SDV)
  • Trial Master File (TMF) maintenance
  • Investigator and site staff training

Nice-to-have

  • Cross-functional project team participation
  • Diplomacy and respect for others
  • Influencing study site staff
  • Organizational and departmental process improvement

Key Requirements

  • Bachelor's degree or higher
  • ICH/GCP guidelines knowledge
  • 21 CFR part 812 knowledge
  • 1+ years CRA experience (CRA)
  • 5+ years CRA experience (Sr CRA)
  • Experience with EDC and eTMF systems

Work Rights

Not specified

Tailored Resume

Cover Letter