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.