Clinical Research Associate, French-speaking
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Job Description
Clinical Research Associate responsible for overseeing clinical trials from Phase I to IV at IQVIA. Collaborating with site staff to ensure compliance with study procedures and best practices.
Responsibilities:
- Participates in the preparation and conduct of Phase I to IV clinical trials
- Oversees the progress of clinical investigations by conducting evaluation, initiation and close-out visits
- Ensures monitoring of clinical trials in accordance with Good Clinical Practice (GCP)
- Collaborates with the ISS team to coordinate activities with the site in preparation for study start-up
Requirements:
- Minimum of 3 years of monitoring experience
- Strong knowledge of the clinical research process
- Four or more years of experience in oncology and/or medical devices
- Excellent written and verbal communication skills
- Ability to manage multiple priorities across multiple, complex trials
- BS/BA/BSc (or equivalent) in a life sciences or healthcare-related field
Benefits:
- Incentive plans
- Bonuses
- Other forms of compensation
- Health benefits
- Wellness programs
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