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Clinical Research Associate II

Posted 22 hours 5 minutes ago by IQVIA LLC

Permanent
Full Time
Research Jobs
Dublin, Ireland
Job Description

IQVIA UK's cFSP team is seeking experienced Clinical Research Associates in Ireland.

Responsibilities
  • Perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • May support start up phase.
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
  • Requires at least 2 years on site monitoring experience of interventional studies.
  • Degree in a scientific discipline or health care or equivalent industry experience.
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Ability to establish and maintain effective working relationships with coworkers and clients.
  • This position is not eligible for visa sponsorship.

Thank you for your interest in growing your career with us.

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