Medical Writer jobs in Hyderabad, Telangana
- SanofiHyderabad, Telangana
- Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis.
- Stakeholders: 1) Work closely with medical teams in…
- Syneos - Clinical and Corporate - ProdHyderabad, Telangana
- Compiles, writes, and edits medical writing deliverables, and serves as medical writer within and across departments with moderate supervision.
- ParexelHyderabad, Telangana
- Solid understanding of global pharmacovigilance regulations, medical terminology, and safety-related concepts.
- AXIS ClinicalsMiyapur, Hyderabad, Telangana
- Reports to Manager / Head of the Department.
- Study design and protocol development.
- Review of study protocols & ICF documents according to regulatory guidelines…
- Syneos - Clinical and Corporate - ProdHyderabad, Telangana
- Compiles, writes, and edits medical writing deliverables, and serves as a medical writer within and across departments with minimal supervision.
- SanofiHyderabad, Telangana
- Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis.
- Stakeholders: 1) Work closely with medical teams in…
- OnTarget CommunicationsHyderabad, Telangana
- Experience in medical devices, healthcare software, biotech, or pharmaceuticals.
- We're looking for a Senior Technical Writer with 6-12 years of experience to…
- Syneos - Clinical and Corporate - ProdHyderabad, Telangana
- Guidelines that affect medical writing.
- Associated with individual studies, defining document strategy and coordinating medical writing.
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- サイネオス・ヘルスMadhapur, Hyderabad, Telangana
- Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal…
- Alchemy Medicine Pvt LtdBanjara Hills, Hyderabad, Telangana
- Prepare compile and coordinate regulatory documents & submissions ( ROW ).
- Manage preparation of CTD, variations, renewals, responses to deficiencies, and other…
- SanofiHyderabad, Telangana
- Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree.
- Process: (1) Develop complex publications material; (2) Act as an…
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- Susoft SolutionsSaidabad, Hyderabad, Telangana
- We have urgent openings for Sr. Medical Transcriptionist and Sr. Proof readers with at least 3+ years experience.
- Susoft SolutionsSaidabad, Hyderabad, Telangana
- We have urgent openings for Sr. Medical Transcriptionist and Sr. Proof readers with at least 3+ years experience.
- R1 RCM, Inc.Hyderabad, Telangana
- Experience of working as a medical transcriptionist/editor on a variety of medical specialties and work types.
- Must have excellent time management skills.
- SanofiHyderabad, Telangana
- Help in coordination of medical events and advisory boards and other medical events, as appropriate.
- Responsible for project management support to the…
- JeevanHyderabad, Telangana
- A certificate in regulatory affairs and/or medical writing is highly preferred.
- Minimum of 2-4 years of relevant industry experience in medical/regulatory…
Job Post Details
Job details
Full job description
Our Team:
Sanofi Business Operations is an internal Sanofi resource organization based in India and is set up to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally.
Main responsibilities:
Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues. Achieved through a combination of product knowledge, along with editing, writing, and document management proficiency.
Essential Job duties and responsibilities: 1) Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature. 2) Generates evidence-based, accurate, current, and fair-balanced summaries of data for the creation/maintenance of scientific response documents for products in designated therapeutic area(s). 3) Adapts global scientific response documents for assigned countries. 4) Develops responses to escalated inquiries for assigned countries. 5) Develops contributions to US NDA Annual Reports. 6) Contributes to US compendia reviews. 7) Ability to execute the MI projects once they are conceptualized with guidance from experienced team members or mangers 8) Demonstrates resolve and urgency to accomplish tasks under the guidance of supervisor. Participate in cross-functional project teams as needed. Ensure that assigned projects are completed on schedule. 9) Develops and maintains Therapeutic Area expertise. 10) Able to conduct quality checks on peer outputs in case of business need11) Collaborates effectively with Global Medical Information teams to execute content plans
People: 1) Maintain effective relationships with the end stakeholders (Medical scientific community) within the allocated Global business unit and product – with an end objective to develop medical information content as per requirement. 2) Interact effectively with stakeholders in medical and pharmacovigilance departments. 3) Constantly assist other medical information writers in developing knowledge and sharing expertise.- Performance: Provide deliverables (scientific response documents, US NDA Annual Reports, US compendia reviews) as per agreed timelines and quality
- Process: 1) Can work with minimum supervision to conduct data sanity and produce error free MI project outputs for countries supported. 2) Assist the assigned medical information team in conducting a comprehensive medical writing needs analysis. 3) Implement relevant elements of content plans and associated activities for the year identified for the assigned countries. 4) Work with selected vendors within the region to deliver the required deliverables as per the defined process. 5) Help to manger to design an overall plan of action basis end-customers feedback & improve course content and delivery.
- Stakeholders: 1) Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables. 2) Liaise with the Medical department to prepare relevant & customized deliverables.
About you
Experience: 2 – 3 years of experience in medical writing for the pharmaceuticals/ healthcare industry or equivalent experience in a clinical setting; At least 1 – 2 years of direct medical information experience in a pharmaceutical company- Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment.
- Technical skills: As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills, Knowledge about literature evaluation and multilevel response development)
- Education: Advanced degree in life sciences/ pharmacy/ similar discipline, Master in science, MBA or equivalent)
- Languages: Excellent knowledge of the English language (spoken and written)