We’re looking for a highly organized and self-driven Clinical Research Coordinator (CRC) to support clinical trial execution across partner hospitals centres. In this role, you will be responsible for end-to-end sample and patient data management, ensuring all site-level trial activities are conducted in alignment with study protocols, regulatory standards, and operational timelines.
This role requires hands-on coordination at the study site working closely with physicians, patients, and internal teams to oversee participant recruitment, informed consent, sample collection, and accurate documentation of clinical data. You’ll play a key role in implementing and maintaining study logs, ensuring equipment functionality, and facilitating timely sample shipments and record-keeping.
A core part of your responsibility will also include maintaining regulatory compliance and ensuring adherence to ICH GCP, SOPs, and institutional guidelines. You’ll act as a point of contact between the site and study teams, keeping stakeholders informed and aligned.
This is a field-facing, people-centric role that demands clear communication, attention to detail, and a commitment to clinical quality. You’ll be encouraged to contribute proactively to process improvements and cross-site collaboration.