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Freelancer Experienced Medical Writer

Capsid Medical Communications

Senior Medical Writer Medical Writer Scientific Writer
We are looking for experienced medical/scientific writers, who can write manuscripts (original, narrative review, systematic review, and meta-analysis) without any support. The candidate should have at least published minimum 3-10 original research/ systematic review / narrative review or meta-analysis in SCI journals.Qualification: Ph.D., M.B.B.S, BDS, M.Pharma, M.ScExperience: 2-5 YearsRoles and Responsibilities:1. Develop manuscript for high impact factor journals in the field of clinical, medical and public health domain of different therapeutic areas2. Excellent Time and Project management skills3. Ability to edit/format the scientific manuscripts as per the journal styles and guidelines4. Ability to do meta-analysis and write systematic review5. Awareness about publication ethics, ICMJE and GPP guidelines 6. Excellent written and verbal communication7. Please do not apply if you havent published articles in high impact factor journals in the field of medical research
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Jr Medical Writer

Mediclin Clinical Research

  • 1 - 3 yrs
  • 4.5 Lac/Yr
  • Mira Road Mumbai
Protocol Clinical Study Report ICF CRF Manuscript Regulatory Writing Medical Writer Walk in
1. Drafting & Preparation of Phase I, II, III & IV protocol,synopsis, PIS for various therapeutic areas such asrespiratory, diabetes mellitus, pain, antimicrobials,cardiovascular and other specialties for India and globalsubmissions.2. Writing CSR, IBs, SmPCs, PIs, PILs.3. Project assignment and timeline to CRAs -Operation team,discussion with KOL and finalization of scientific studyDocuments as per requirements4. Literature search, systemic review of data and its analysis soas to be up to date with latest breakthrough in the therapeuticarea.5. Working closely with physicians and senior scientists forstudy designs and protocol development to influence theclinical pharmacology strategy in support of drugdevelopment.6. Preparing presentations, posters, research articles, abstract,and manuscripts for publication purpose.7. Activities as and when required.
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Senior Medical Writer

Mediclin Clinical Research

  • 3 - 5 yrs
  • 6.0 Lac/Yr
  • Mira Road Mumbai
ICF CRF Manuscript Protocol Clinical Study Report Regulatory Writing Medical Writer Walk in
1. Drafting & Preparation of Phase I, II, III & IV protocol,synopsis, PIS for various therapeutic areas such asrespiratory, diabetes mellitus, pain, antimicrobials,cardiovascular and other specialties for India and globalsubmissions.2. Writing CSR, IBs, SmPCs, PIs, PILs.3. Project assignment and timeline to CRAs -Operation team,discussion with KOL and finalization of scientific studyDocuments as per requirements4. Literature search, systemic review of data and its analysis soas to be up to date with latest breakthrough in the therapeuticarea.5. Working closely with physicians and senior scientists forstudy designs and protocol development to influence theclinical pharmacology strategy in support of drugdevelopment.6. Preparing presentations, posters, research articles, abstract,and manuscripts for publication purpose.7. Activities as and when required.
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Medical Writer

Alpha MD Pvt Ltd

  • 4 - 7 yrs
  • Mumbai
Clinical Research Medical Affairs Drug Safety Clinical Operations Medico Marketing Medical Writer SOP CRO KOLs Protocol Writing Manuscript Abstract Healthcare
Job Description: Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract, Review articles and Medico-marketing inputs) Should be able to develop LBL, Poster, News-letters, KOL cases, booklets, atlas, guideline booklet, product monographs, calendars, compendium, customized journals, handbooks, conference abstract booklets, yearbooks, KOL opinion booklets, case studies, CMES, etc. Should have hands on experience in literature search and systematic review Should be accountable for medical writing deliverable and should ensure work on assigned projects adheres to industry/international standards Should be able to draft article on Health Economic Outcome Research and understanding on subject will be added advantage Should be responsible for continual improvement of in-house medical writing capabilities Should have an excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards. Should liaise with internal team, clients, authors and KOLsExperience: Min 4 - 7 years experienceQualification: Bachelors degree / Masters Degree in any Pharma / Lifesciences/ Science related field. Excellent verbal and written skills (English). Good organizational, interpersonal, and team skills. Ability to deliver results under pressure. Goal oriented, self-motivated; able to work independently but within a team environmentDesired Skills/Experience: A good understanding of the healthcare market, challenges, growth prospects and healthcare delivery operations Strong customer and contact network in healthcare domain A minimum of three five years medical writing experience within the pharmaceutical industry or a contract research organisation. Able to work independently, initiate their own projects as needed to streamline their wo
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