Overview
Clinical Trial Coordinator Jobs in Port Louis, Mauritius at CENTRE D’ETUDES CLINIQUES
Title: Clinical Trial Coordinator
Company: CENTRE D’ETUDES CLINIQUES
Location: Port Louis, Mauritius
Company Description CENTRE D'ETUDES CLINIQUES is a Contract Research Organisation located in Port Louis, Mauritius. The organization focuses on clinical study activities that support improved healthcare practices and outcomes. It operates within a collaborative environment, working with healthcare professionals and partners to conduct and oversee clinical projects. Team members contribute to initiatives that advance clinical knowledge while maintaining high ethical and regulatory standards.
Role Description The Clinical Trial Coordinator is a full-time, on-site role based in Port Louis. The individual in this role will coordinate the day-to-day conduct of clinical trials, including scheduling participant visits, maintaining study documentation, and ensuring adherence to approved protocols. Responsibilities include supporting patient recruitment and screening, obtaining and organizing informed consent documents, and collecting, entering, and verifying clinical data. The coordinator will collaborate with investigators, site staff, and sponsors to ensure regulatory and ethical compliance, prepare trial-related reports, and assist with monitoring visits and audits. The role also requires tracking project timelines, identifying operational issues, and contributing to continuous improvement of clinical trial processes.
Qualifications
- Strong Communication skills, including the ability to interact effectively with participants, investigators, and multidisciplinary teams.
- Proficiency in Protocol adherence and understanding of clinical trial procedures and regulatory requirements.
- Demonstrated Research skills, including data collection, documentation, and basic data analysis.
- Hands-on experience or academic exposure to Clinical Trials operations and Good Clinical Practice (GCP) standards.
- Solid Project Management abilities, such as organizing tasks, managing timelines, and coordinating multiple trial activities.
- Relevant degree or diploma in life sciences, nursing, pharmacy, public health, or a related field.
- Attention to detail, strong organizational skills, and a high level of integrity and ethical judgment.
- Comfort working on-site in a clinical setting in Port Louis; prior experience in a clinical or research environment is an asset.
