About This Role
The Clinical Research Coordinator supports a clinical research site, performing administrative and clinical tasks to ensure the smooth execution of clinical trials. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Responsibilities
- Maintain and update study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
- Support patient screening and enrollment, including handling informed consent and privacy documentation
- Coordinate logistical activities for study procedures in line with the study protocol
- Perform data entry, quality checks, and resolve queries to ensure data accuracy and completeness
- Patient education
- Communicate with study monitors and respond to study-related inquiries
- Carry out general administrative tasks related to the study
Requirements
- Bachelor
’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
- Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
- Good knowledge of medical terminology
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- At least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
- Excellent interpersonal and communication skills
- Strong organizational skills and attention to detail
- Fluency in French and good command of English
Important Details
- Schedule: Part-time, 24 hours per week
- Duration: Approximately 6 months
- Start date: Immediately
About the Company
IQVIA is a global team that is advancing healthcare through data, technology, and human science.
