Associé de recherche clinique – Francophone – IQVIA Clinical Research Associate – French speaking
| Company | IQVIA |
|---|---|
| Location | Montreal, QC, Canada, Quebec City, QC, Canada |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Senior |
Requirements
- 3 years of experience in follow-up
- BS/BA/BSc (or equivalent) in one of the life sciences or healthcare fields
- Experience in monitoring and/or coordinating clinical trials is mandatory
- Strong knowledge of the clinical research process, including working knowledge of clinical trial functional areas and medical terminology
- Excellent written and verbal communication skills to express complex ideas to study staff in research and clinical institutions
- Ability to manage multiple priorities across multiple and complex trials
- Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research
- Computer skills, including proficiency in Microsoft Word, Excel, and PowerPoint and the use of a laptop
Responsibilities
- Participates in the preparation and execution of Phase I to IV clinical trials
- Oversees the progress of clinical investigations by conducting interim site assessment, initiation, and closure visits
- Monitors clinical trials in accordance with clinical best practices and procedures established by IQVIA and its sponsors
- Collaborates with ISS to coordinate activities with the site in preparation for the launch of the study
- Conducts study initiation activities, reviews protocol, regulatory issues, study procedures with site staff, and provides training at the end of FERC
- Ensures adherence to good clinical practices, investigator integrity, and adherence to study procedures through on-site monitoring visits
- Documents the responsibility, stability, and storage conditions of clinical trial material as required by the sponsor
- Examines the quality and integrity of clinical data through internal review and on-site source verification
- Serves as the primary contact between IQVIA and the investigator; coordinates all correspondence
- Conducts study closure visits in accordance with the study-specific clinical follow-up plan
Preferred Qualifications
- Previous experience in a clinical research organization (CRO) preferred
- Previous project team leadership experience preferred
- Working knowledge of budget management preferred
- Experience in organization of clinical research (ORC) preferred