Prepare and review of CSR, appendices and other relevant documents (bio summary tables, module 2.7, CS-BE etc.) as per the regulatory/sponsor requirements in the required format.
Coordinate with all concerned department to ensure timelines and compliance to regulatory/sponsor requirements for preparation, compilation and delivery of reports.
Preparation of study reports for CE/PK studies, Brand studies
Attend to medical writing related sponsor queries.
Prepare amended reports and amendments to the CSR when necessary.
Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.
Providing coding for all adverse events recorded in the study as per MedDRA coding system for clinical trials.
Attend to medical writing related sponsor queries.
Quality check of the final compiled study reports for delivery.
Responsible for providing practical training to new recruits regarding the preparation of CSR, appendices and other relevant documents.
Report to Lead Medical Writing-Reports.
To carry out other responsibilities as and when assigned by management.
System improvements as required on day-to-day basis as per business requirements.
Mentor team and as assigned, act as subject matter expert (SME)
Project lead when assigned
Your experience and qualifications
Experience : 8+ years in writing reports/technical operations