Clinical Research Associate - Clinical Operations

Job Description

• Explores new prospective sites and conductingfeasibility survey for the studies
• Assists CPMs in studying start-up activities,regulatory process and execution of studyrelated agreements
• Prepares visit reports as per SOPs after each sitevisit.
• Maintains ongoing communication with sites toprovide information, queries resolution, andreview overall progress of clinical trials andadherence to established guidelines.
• Keeps the CPMs updated with the study status atsites
• Ensures the correct storage, handling and use ofinvestigational product in accordance with SOPs.
• Supervises the CTA in maintaining and updatingtrial master files on regular basis; Responsiblefor ensuring compliance to GCP, applicable SOPsand applicable regulatory requirements.
• Performs other study related tasks as assignedby Clinical Project managers

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