Scientific Writer
3 days ago
About Clinforge
Clinforge Clinical Research Solutions Pvt. Ltd. is a growing Contract Research Organization (CRO) dedicated to delivering high-quality services in
clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing
. Our mission is to bridge science and communication by transforming complex research into impactful knowledge.
Key Responsibilities
- Develop, write, and edit
scientific manuscripts, review articles, case studies, and conference abstracts/posters
. - Prepare
regulatory and clinical documents
(clinical study reports, investigator brochures, patient information leaflets, regulatory dossiers). - Create
medical communication materials
including slide decks, CME content, and white papers for healthcare professionals. - Collaborate with researchers, clinicians, and regulatory teams to ensure
accuracy, consistency, and compliance
with journal/regulatory requirements. - Conduct
literature reviews
and ensure referencing accuracy (PubMed, Scopus, etc.). - Ensure documents follow
ICMJE, GCP, CONSORT, and journal-specific guidelines
. - Maintain high standards of
clarity, accuracy, and scientific integrity
.
Qualifications & Skills
- Master's or PhD in
Life Sciences / Pharmacy / Biotechnology / Clinical Research
. - 1–3 years of experience in
scientific or medical writing
(Fresher with strong writing skills may be considered). - Strong command of
English language, grammar, and scientific terminology
. - Familiarity with
journal submission processes
and reference management software (EndNote, Mendeley, Zotero). - Knowledge of
regulatory writing
(CSR, CTD/eCTD modules) will be an added advantage. - Excellent communication, attention to detail, and ability to meet deadlines.
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