Narrative Medical Writing Role
2 weeks ago
Job Description Responsibilities: 1. As per process requirement and assigned primary responsibility, support narratives (draft and QC) 2. Ensure that the narratives are in accordance with the client SOPs, guidelines and agreed timelines and comply with client quality standards 3. Perform Quality check of the narratives according to the project specific checklist and against the source documents such as patient listing, concomitant medication listing, CIOMS form etc. and log defect in the defect tracker after analyzing the defect category 4. Conduct and attend narrative kick-off meeting with client to understand the project requirements such as scope of the project, narrative writing plan, narrative categorization. 5. Prepare guidance/convention document for drafting narratives in accordance with the client requirements that must be followed by the team members for consistency within narrative project. 6. Conduct and attend comment resolution meetings with the Clinical lead/safety scientist to seek comment clarification and provide probable solution for conflicting comments. 7. Perform scientific review of the narratives drafted and QCed by the team. 8. Perform tracking of large volume of narratives through narrative tracking sheet to understand process stage of the narrative and provide allocations to the team. 9. Mentoring and coaching the junior writers on their tasks in completing and finalizing their narrative writing deliverables with the defined quality and timeline. 10. Initiate and implement process improvement projects 11. Complete assigned (TCS/Client) trainings within stipulated timelines 12. Provide timely data (study tracker, quality metrics, billing numbers/effort hours) forpreparing relevant (e.g. quality, TAT, effort hours, etc.) and project status updates, as defined by the TCS/client requirements 13. Conduct knowledge sharing sessions based on acquired knowledge for team excellence and process improvement
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Narrative writing
6 days ago
Bengaluru, Mumbai, Noida, India Tata Consultancy Services Full time ₹ 6,00,000 - ₹ 12,00,000 per yearTCS is Hiring - Narrative writinglocation - Mumbai, Noida, BengaluruExperience Range - 5 to 10Interested Candidate can mail on - Preferred Educational Qualification for the role - Any life science Postgraduate, BDS, MDSSkills: CSR narrative, common technical document, clinical study report, Narrative writing, investigator brochure, protocol writingJob...
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Pharma SME
3 weeks ago
Mumbai, India UsefulBI Corporation Full timeWe are hiring Pharma SME - Medical Writing Experience: 5-8 years Industry: Pharmaceutical Shift Timing: 2 pm to 11 pm Locations: Pune/Bangalore/Lucknow Key Responsibilities: - Develop, review, and finalize scientific and regulatory documents including clinical study reports (CSRs), protocols, investigator brochures (IBs), and safety narratives. - Ensure all...
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Medical Writing
2 weeks ago
Mumbai, India Tata Consultancy Services Limited Full timeJob Description 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...
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Medical Writer Ii
1 day ago
Navi Mumbai, Maharashtra, India Fortrea Full time**Job Overview**: Lead writer responsible for preparation of clinical study protocols and clinical study reports (CSRs), and other clinical documents as needed. Provides support to more experienced writers with the preparation of complex clinical documents. Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate....
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Medical Content Writer
3 days ago
Airoli, Navi Mumbai, Maharashtra, India Neural IT Full time**Designation: Medical Content Writer** **Qualification: Bpharm / Mpharm** **.Experience: 2 yrs** **Skills Required**: - Good vocabulary and grammar knowledge for effective medical report writing. - Clear, concise, scientific style of writing with a high level of attention to detail. - 2-3 years of experience as a Medical Record Reviewer. **Roles &...
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Team Member
2 weeks ago
Mumbai, India Cipla Full time**Division**: - IPD**Department**: - IPD**Employment Type**: - Permanent**Job Purpose**: Develop and review clinical documents for regulated and non-regulated markets ensuring regulatory compliance and thus assisting on-time product registration and renewal **Accountabilities**: 1. Develop and review documents for clinical and bioequivalence studies to...
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Medical Content Writer
1 week ago
Airoli, Navi Mumbai, Maharashtra, India Neural IT Full timeDesignation: Medical Content WriterQualification: A degree in life sciences or pharmacology.Experience: 1 to 2 yrsSkills Required: - Good vocabulary and grammar knowledge for effective medical report writing. - Clear, concise, scientific style of writing with a high level of attention to detail. - 1-2 years of experience as a Medical Record...
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Medical Writer
2 weeks ago
Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time**Title**:Medical Writer**: - Date: Jun 6, 2025 - Location: Sun House - Corporate Office - Company: Sun Pharma Laboratories Ltd **Job Summary**: This role will responsible for preparation of clinical high-quality protocol, investigator brochures, regulatory documents, data review, clinical study report, publications, and related clinical documents....
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Head of Strategic Narrative
2 weeks ago
Mumbai, India Persistent Systems Full timeAbout Position: The Head of Strategic Narrative & Thought Leadership will define and drive Persistent's voice in the market - connecting our technology vision, delivery excellence, and innovation culture into a unified global story. The role blends strategic storytelling, editorial excellence, and market insight, ensuring Persistent's narrative is...
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Medical Writer
2 weeks ago
Goregaon, Mumbai, Maharashtra, India Pink Sky HR Services Full time**Job Summary**: **Key Responsibilities**: - **Content Development**: - Create, write, and edit clinical study reports, patient narratives, manuscripts, regulatory documents (such as Clinical Study Protocols, Investigator’s Brochures, and Clinical Study Reports), and other scientific documents. - **Regulatory Submissions**: Assist in the preparation of...