IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. They are seeking a Clinical Research Associate to perform site selection, monitoring, and close-out visits while ensuring the quality and integrity of site practices.
Responsibilities
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Skills
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
- An equivalent combination of education, training and experience
- Good basic knowledge of applicable clinical research regulatory requirements
- Comfortable collaborating and communicating with a variety of colleagues and customers
- 2 years of clinical research coordinator experience strongly preferred
Benefits
- Incentive plans
- Bonuses
- Health and welfare benefits
Company Overview
IQVIA provides analytics, compliance, and management solutions to the life sciences industry. It was founded in 1982, and is headquartered in Danbury, Connecticut, USA, with a workforce of 10001+ employees. Its website is https://www.iqvia.com.
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