Clinical Research Coordinator

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.

Requirements

Bachelor’s degree in life sciences, nursing, pharmacy, or a related healthcare field. 1–3 years of

experience

in clinical research or patient-facing roles. Strong familiarity with clinical trial documentation, SOPs, and protocol workflows. Comfortable working in a hospital or field setting;

experience

handling clinical samples preferred. Excellent organisational

skills

and attention to detail. Strong communication and interpersonal skills, especially with physicians and patients. Ability to work independently, manage timelines, and follow through on operational tasks.

Bachelor’s degree in life sciences, nursing, pharmacy, or a related healthcare field. 1–3 years of

experience

in clinical research or patient-facing roles. Strong familiarity with clinical trial documentation, SOPs, and protocol workflows. Comfortable working in a hospital or field setting;

experience

handling clinical samples preferred. Excellent organisational

skills

and attention to detail. Strong communication and interpersonal skills, especially with physicians and patients. Ability to work independently, manage timelines, and follow through on operational tasks.