Day-to-day responsibilities include reviewing and understanding study protocols, assisting in site selection and activation, tracking regulatory and logistics milestones, and maintaining trial documentation and reports. The role also involves collaborating with cross-functional teams to manage clinical supplies, supporting site training and communication, and proactively identifying and resolving operational issues. The CRA will contribute to process improvement initiatives and support consistent application of Intrinseque Health’s project management methodologies across assigned studies.
Qualifications
- Candidates should possess strong knowledge of clinical trial protocols and related documentation.
- Candidates should possess experience working as Clinical Research Associates and supporting study monitoring activities.
- Candidates should possess practical understanding of clinical trials and Valuable Clinical Practice (GCP) guidelines.
- Candidates should possess skills in research and data review to support evidence-based decision-making.
- Candidates should possess familiarity with clinical operations, including site management, logistics coordination, and regulatory processes.
- Relevant degree in life sciences, pharmacy, nursing, or a related field.
- Strong organizational, time-management, and project coordination abilities.
- Clear written and verbal communication skills and the ability to work effectively in cross-functional teams.