Clinical Research Associate

Clinical Research Associate
  • Competitive
    HOUR
  • Permanent
  • Morrisville NC, US Morrisville WAKE US 27560
Job Ref: JO000112061
Sector: Clinical
Sub-sector: Clinical
Date Added: 04 March 2021

Senior Clinical Research Associate

  • Perform monitoring and site management activities for Phase I - IV clinical research projects to assess the progress of clinical projects at assigned investigative / physician sites to ensure clinical projects are conducted, recorded, & reported in accordance with protocol.
  • Perform site qualification, site initiation, interim monitoring, site management and close-out visits ensuring regulatory, ICH-GCP and / or GPP and protocol compliance.
  • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
  • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject / patient as required / appropriate.
  • Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
  • Other duties / responsibilities as assigned.

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRGTalent
31/03/2021 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Melissa Rodrigues

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