Medical Writer

Veeda Lifesciences is seeking a Medical Writer With a relevant experience in Clinical Trials.This is a full-time job, With a flexibility of Hybrid Working.Job Requirements: B-Pharm, M-Pharm, Pharm- D or relevant field At least of 2 Years working experience in the field Excellent command of spoken and written English Ability to work independently but also as part of the team with minimal supervision Ability to work with multiple priorities and tight deadlinesMain role and responsibilities: Ct documents like protocol / CSR for patient based CT involving molecules for regulated market Preparation & Review of Protocol, ICD, Synopsis and other study specific documents e.g. patient diary card. Preparation & Review of Investigator Brochure. Evaluating trial feasibility (preliminary and detailed) for patient based clinical studies along with medical team for various regulatory submissions. To support in reference literature search as required for assigned projects. Providing the Protocol Training to Monitors and site team if required. Preparation & Review of Clinical study report (CSRs) for phase trials conducted by Clinical Operations Department of Veeda as per regulatory requirement and define timeline in project grid - Study execution sheet in coordination with the Project Manager. Preparation & Review of Full CSRs, Abbreviated CSR, Synoptic CSR, Shell and Interim report as per Sponsor necessity. Preparation and finalization of clinical study report and related appendices/documents for adequacy to be submitted as part of CTD/eCTD as per applicable regulatory requirements. Review of statistical analysis plans, mock shells and table/figure/listing specifications for appropriate content. Perform literature searches/reviews as necessary to obtain background information and development of documents. Compliance to sponsor audit and regulatory inspections (e.g., USFDA, EMA, DCGI etc.) and query/deficiencies reply. To ensure and improve quality & presentation of report through writing, editing and/or managing the production of high-quality clinical documentation (e.g., Study Report, Summary Documents and ensure compliance of documentation to internal company standards and external regulatory guidelines). Preparation and review of departmental SOP and other departmental SOPs as required. Ensure that the reports and appendices and related material are archived / e-archived in a timely manner. Preparation of project summary and submit to reporting head/designee Develop and maintain the necessary templates, formats and styles to ensure that documents generated meet the industry, internal, client & regulatory requirements. Participate in departmental or interdepartmental process improvement and training initiatives.

Apply Now