IQVIA is seeking a Site Research Assistant for a clinical study in Grenoble, requiring 16 hours per week for a duration of approximately 6 months. The role involves supporting clinical trial operations, maintaining study documentation, and ensuring safety protocols are followed
Job Summary
The role involves supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.
Candidates will be responsible for administrative tasks including data entry, quality checking, and managing biological samples to ensure smooth trial operations.
This is a 16 hours per week position expected to last around 6 months starting at the beginning of April.
Matching Summary
Match Score: 85
IQVIA is seeking a Site Research Assistant for a clinical study in Grenoble, requiring 16 hours per week for a duration of approximately 6 months. The role involves supporting clinical trial operations, maintaining study documentation, and ensuring safety protocols are followed.
Skills & Requirements
Must-have
Maintain up-to-date study protocols
Screen and enrol patients for trials
Data entry and query resolution
Manage and ship biological samples
Coordinate with study monitors
Nice-to-have
Excellent interpersonal skills
Strong organizational abilities
Ability to pay close attention to detail
Key Requirements
BS/BA in life sciences or equivalent
1-2 years experience as Clinical Research Assistant or Coordinator
Fluent French language skills
Good knowledge of clinical trials and operating procedures