As a Clinical Research Specialist, you will support one or more clinical studies within the Clinical R&D department, collaborating with internal and external stakeholders to ensure compliance with guidelines and achievement of study milestones.
Key Responsibilities:
Support the feasibility, initiation, conduct, and closure of clinical trials.
Act as the primary point of contact for clinical trial sites, assisting with documentation (study protocols, informed consents, monitoring plans, etc.).
Coordinate and manage investigational devices, trial materials, and budgets.
Contribute to the development of study reports and data analysis for publications.
Conduct monitoring activities, including site visits, data collection, and protocol compliance, as needed.
Collaborate with investigators, ethics committees, and vendors to ensure smooth study execution.
Provide safety coordination during clinical studies, including the reporting of safety data and adverse events.
