What are the responsibilities and job description for the CRA2/SCRA position at IQVIA?
CRA2/SCRA needed for IQVIA. All talented candidates are welcome to apply.
THE ROLE:
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with Good Clinical Practice
• Administer protocol and related study training to assigned sites
• Manage the progress of assigned studies by tracking regulatory submissions and approvals.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
• Collaborate and liaise with study team members for project execution support as appropriate.
REQUIREMENTS:
• Bachelor's Degree in scientific discipline or health care preferred.
• A minimum of 2 years' on-site monitoring experience.
• Good knowledge of, and skill in applying Good Clinical Practice (GCP) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Interested? Then apply right now!
Clintec, an IQVIA company, is an innovative global functional services provider with a depth of expertise in oncology and rare diseases. https://jobs.iqvia.com/clintec-careers
