Clinical Research Associate overseeing Phase I - IV clinical trials at IQVIA. Collaborating with site staff to ensure study compliance and data integrity while supporting global clients.
About the role
- Clinical Research Associate ensuring sites conduct studies and reporting data accurately. Monitoring, site management, and collaboration with the study team.
Responsibilities
- Perform monitoring and site management work to ensure that sites are conducting the study(ies)
- Perform site monitoring visits
- Work with sites to adapt, drive and track subject recruitment plan
- Administer protocol and related study training
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure copies/originals site documents are available for filing in the Trial Master File
- Create and maintain appropriate documentation regarding site management
- Collaborate and liaise with study team members for project execution support
Requirements
- Bachelor's Degree in scientific discipline or health care preferred
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Some organizations require completion of CRA training program or prior monitoring experience.
- Basic knowledge of applicable clinical research regulatory requirements.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Benefits
- health and welfare and/or other benefits
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