Job Description:
Preparing case studies, medical abstract writing, medical write - ups for media publishing and Newsletter under the guidance of the Chief Scientific Officer & Technical Director.
Preparing Manuscript for publishing.
Preparing market report, product monograph, ppt.
Managing, Coordinating & Maintaining Intellectual Property trademark, copyright of existing and new product.
Meeting the statutory body as and when required.
Adhering to SOPs, regulations, good clinical and ethical practices and protocol procedures
Coordinating between sponsors, investigators and CRO
Facilitate monitoring
Schedule patient visits and follow-up visits
Investigational product storage and accountability
Maintenance and completion of study files
Coordination with Data Management and resolution of queries
Completion and verification of source documents
Monitoring and verification of essential documents (Protocol, CRF, ICF, etc)
Communicating with Ethics Committee for submission of study related reports
Maintaining subject screen logs and protocol deviation logs
Maintaining spreadsheet tracking updates of database of all clinical trial related activities
Communicate with central laboratory for logistics/shipment from investigator sites
Carry out any other job-related activities as and when deemed necessary
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