Description
As a Clinical Research Associate at IQVIA, you will perform monitoring and site management work to ensure that sites are conducting studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Your responsibilities will include:
- Performing site monitoring visits in accordance with contracted scope of work and Good Clinical Practice
- Working with sites to adapt, drive, and track subject recruitment plans
- Administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of study site practices
- Managing the progress of assigned studies
- Ensuring site documents are available for filing in the Trial Master File
- Creating and maintaining documentation regarding site management and monitoring visit findings
- Collaborating with study team members for project execution support
You will need:
- A Bachelor's Degree in a scientific discipline or healthcare
- At least 2 years of independent on-site monitoring experience as a Clinical Research Associate
- Good knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice and International Conference on Harmonization guidelines
- Therapeutic and protocol knowledge
- Computer skills, including proficiency in Microsoft Word, Excel, and PowerPoint
- Experience utilizing EDC, CTMS, eTMF, IVRS/IWRS, and other clinical trial systems
- Excellent written and verbal communication skills
The potential base pay range for this role, when annualized, is $74,500.00 - $197,500.00.