Medical Writer
23 hours ago
Position: Senior Medical Writer – RWELocation: Bangalore Job Type: Full-time Department: Medical Writing – MCAPLJob DescriptionThe Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the ability to lead real-world evidence (RWE) and epidemiological studies that support clinical and regulatory objectives.Key ResponsibilitiesAuthor, edit, and review a wide range of documents including clinical protocols, study reports, investigator brochures (IBs), regulatory submissions, manuscripts, abstracts, and presentation materials.Design and lead real-world data and epidemiological studies (protocols, data collection, analysis, and interpretation) to assess disease trends, health outcomes, and risk factors.Support regulatory submissions and deliver study reports, publications, and presentations.Translate complex scientific and clinical findings into clear, audience-specific content for regulators, sponsors, patients, and healthcare professionals.Conduct comprehensive literature reviews to support evidence-based writing and ensure scientific accuracy.Collaborate with cross-functional teams (clinical, regulatory, medical, marketing, and technical) to maintain consistency and integrity in scientific messaging.Participate in cross-departmental meetings to align on expectations, gather insights, and support project timelines.Incorporate feedback from internal reviewers, external stakeholders, and quality review processes to refine deliverables.Manage document version control and workflow tracking in accordance with project management systems.Stay updated on therapeutic area advancements, regulatory changes, and best practices in medical writing.Provide technical mentorship, manage project timelines and budgets, and ensure compliance with evolving public health and regulatory standards.Clinical Data Management: Lead eCRF design, data collection, entry, validation, and query management; perform database testing (including UAT); ensure timely delivery of clean, reliable datasets through interim reviews and database lock.Quality and Compliance: Prepare DMPs/DVPs, implement edit checks and reconciliation procedures, coordinate with vendors and cross-functional teams, and maintain compliance with GCP, ICH, and 21 CFR Part 11 while driving process improvements.QualificationsMaster’s degree in Life Sciences, Epidemiology, Public Health, or Biostatistics; Bachelor’s in Medicine, Pharmacy, or related fields (Ph.D., PharmD, or MD preferred).3–5 years of professional experience in medical/scientific writing, applied epidemiology, or public health research within CRO, pharmaceutical, or academic environments.Strong understanding of medical and scientific concepts with the ability to translate complex data into clear, concise documents.Excellent scientific writing, editing, and verbal communication skills with strong attention to detail.Proficient in Microsoft Office Suite and reference management tools (e.g., EndNote, Zotero).Knowledge of statistical software (e.g., SAS, R, Python) and data visualization tools is an advantage.Proven ability to manage multiple projects, meet tight deadlines, and work independently or collaboratively across teams.Preferred AttributesExperience writing in therapeutic areas such as Oncology, Neurology, or Rare Diseases.Track record of publications in peer-reviewed journals or experience supporting manuscripts and conference materials.
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Medical Writer
2 weeks ago
bangalore, India 72 Dragons Full timeWe are looking for a Health Professional (Medicine, biotechnology, pharmacy, nursing, microbiology, dentistry, or biomedical sciences), to join our health writing team. This is a full-time position in India. The candidate must have a health and science background and experience writing in-depth medical content. The writer will be responsible for creating...
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Medical Writer
1 week ago
bangalore, India 72 Dragons Full timeWe are looking for a Health Professional (Medicine, biotechnology, pharmacy, nursing, microbiology, dentistry, or biomedical sciences), to join our health writing team. This is a full-time position in India. The candidate must have a health and science background and experience writing in-depth medical content. The writer will be responsible for creating the...
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Medical Writer
17 hours ago
bangalore, India Trigent Software - Professional Services Full timePosition: Senior Medical Writer – RWE Location: Bangalore Job Type: Full-time Department: Medical Writing – MCAPL Job Description The Senior Medical Writer – RWE will be responsible for authoring, reviewing, and managing high-quality scientific and regulatory documents. The role requires strong scientific understanding, writing expertise, and the...
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Freelance Medical Writer
1 day ago
bangalore, India MIRA Healthcare Full time🚨 Hiring: Freelance Medical Writer (Scientific & Clinical Research Focus)Mira Healthcare is looking for a freelance medical writer to assist in drafting and editing scientific papers, primarily focused on nutraceuticals, probiotics, and microbiology-based research, as well as clinical trials involving nutraceutical interventions.🧠 Role...
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Medical Writer
16 hours ago
bangalore, India PDC CRO Full timePharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region. Our clients include pharmaceutical, biotechnology, medical device industries, other CROs, and academic organizations. Our team is experienced...
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Medical Writer
1 day ago
bangalore, India Biocon Biologics Full timeMedical Affairs Writer JD 1. Writing, editing, reviewing, formatting, publishing regulatory (clinical and post marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and other similar standards. 2. Collaborating with the clinical team in developing and strategizing the Clinical Development Plan. 3....
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Senior Medical Writer
4 weeks ago
Bangalore, Karnataka, India IQVIA Full timeIQVIA is looking for candidates who have expertise in regulatory writing to join our Real World Evidence team The Ideal candidate will have 5-12 years of experience working as Regulatory Medical Writer adept in developing and authoring clinical study protocols informed consent documents clinical study reports Expectations Familiarity with the structural and...
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Medical Writer
1 day ago
bangalore, India PDC CRO Full timePharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region. Our clients include pharmaceutical, biotechnology, medical device industries, other CROs, and academic organizations. Our team is experienced...
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Medical Writer
4 weeks ago
Bangalore, India Jobted IN C2 Full timeOverview: We have an exciting role of Medical Writer - Manager to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global clients, including many Fortune 50 companies. About US We are an integral part of Annalect Global and Omnicom Group, one of...
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Medical Illustrator
1 day ago
bangalore, India DesignMedicine Full timeRole DescriptionThis is a full-time remote, clinical role for a Medical Illustrator. You'll work closely with medical writers, subject matter experts, and designers to create high-quality visuals for a range of medical and scientific content, including:Creating accurate, engaging, and visually appealing illustrations of human anatomy, surgical procedures,...
