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Clinical Research Associate
1 week ago
Clinical Research Associates (CRAs) play a vital role in the success of clinical trials. As a CRA at Heads, you will be responsible for ensuring that clinical trials are conducted according to approved protocols, ICH GCP guidelines, and applicable laws and regulations.
Main Responsibilities:
- Acknowledge and ensure compliance with quality management systems, ICH GCP guidelines, and local/international legislation.
- Conduct pre-study visits at potential investigational sites to evaluate resources and facilities.
- Collaborate with Regulatory Affairs and Clinical Operations staff for clinical submissions and contracts.
- Train and assist investigators in conducting clinical trials.
Requirements:
- Bachelor's or Master's degree in Health Sciences.
- Previous work experience as a CRA desirable.
- Excellent command of English and French both oral and written.
- Ideal candidate should possess good computer skills, organizational skills, and ability to communicate effectively.
