TCS Walk-in Interview 2025.TCS Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: Medical Writing
- Experience:2 – 4 years of experience
- Qualification: BACHELOR OF PHARMACY, BACHELOR OF SCIENCE (B.Sc), M.SC., MASTER OF SCIENCE, MASTER OF SCIENCE (APPLIED PHYSICS)
Important Details :
- Work Location: Mumbai
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description: Greeting from TCS !!!
TCS is hiring for Medical Writing Role!!!
Job Description:
• Setting, discussing and meeting expectations of the document during kick off and subsequent meetings
• Lead the authoring/editing of clinical documents, as mentioned above.
• Ensure adherence to established processes, timelines, regulatory guidelines and applicable standards, styles, guidelines
• Perform quality review of the clinical documents within established timelines with adherence to applicable guidelines, templates, and processes
• Ability to effectively and proactively communicate with internal and external stakeholders, including authors and key opinion leaders as appropriate (including problem-solving and resolution of issues)
• Keep abreast of project status, clinical operating plans and ongoing/new studies as well as scientific literature within assigned project
• Maintain and develop current knowledge of regulatory guidelines, technological advances and industry standards
• Training and mentoring of the new recruits/existing medical writers
• Oversee live projects assigned to the new medical writers and guide them as required
• As required, take on functional role and responsibilities of the role of Documentation Lead –
o Lead PDRD deliverables for project and act as first point of contact for any information that is required for content/document preparation
o Ensure alignment and content re-use across documents for a product
o Onboard lead document writers on document content alignment and timelines.
o Provide required source documents incl. information pertaining to study documentation, relevant project contacts (authors, reviewers), developmental strategy
o Actively participate in Regulatory Affairs Functional or other cross functional team meetings
o Review content of document prior to finalization to ensure high quality prior to initiation of author review or Expert Team Review
