Tata Consultancy Services(TCS) Released Job Openings On 05/12/2022.Tata Consultancy Services is an Indian multinational information technology services and consulting company with its headquarters in Mumbai. It is a part of the Tata Group and operates in 150 locations across 46 countries. In July 2022, it was reported that TCS had over 600,000 employees worldwide..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Tata Consultancy Services(TCS) Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Tata Consultancy Services(TCS) Recruiting B.Pharm Graduate with 01-15+years experience for Medical Writer (PV Role) position.Complete Details for the Medical Writer (PV Role) as follows.
Important Details :
- Location :Mumbai
- Skills: Life Sciences Domain
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 05/12/2022
- Mode of application :Online
- How To Apply: Qualified/interested can send resumes to mallikarjunamocharlla@gmail.com by December-2022 EOM
Related Job: B.Pharma,M.Sc,B.Sc FRESHERS And Experienced Openings At Cilicant Chem For QA,QC,R&D
Job Description/Skills Required
Job Description:
Authoring/editing experience in the medical writing domain across different therapeutic areas in clinical documents including clinical study protocol, pediatric investigational plan, informed consent document, clinical study report, investigator’s brochure, clinical summary of pharmacology, clinical overview (efficacy and safety), briefing package/pre-meeting package and/or safety documents like Development safety update report (DSUR), Periodic benefit risk evaluation report (PBRER), Periodic Adverse Drug Experience Report (PADER/PAER), Risk Management Plans (RMPs), and addendum to clinical overviews (aCOs) preferred
· Experience in preparation of clinical/safety documents necessary for national and international regulatory submissions to the US, European and other regulatory agencies
· Clear, concise and scientific style of writing, with attention to detail
· Strong analytical skills and expertise in writing and review of scientific/clinical/safety documents
· Good knowledge of clinical research domain, ICH GCP principles, Common Technical Document (CTD) structure, and regulatory requirements
· Effective coordination and presentation skills – good organization and time management skills
· Exceptional interpersonal, verbal, and written communication skills
Computer Literate: Knowledge of MS Word, PowerPoint, Adobe Acrobat, MS Excel, etc
