Clinforge Clinical Research Solutions Private Limited

About: ClinforgeClinforge Clinical Research Solutions Pvt. Ltd. is a growing Contract Research Organization (CRO) committed to excellence in clinical research, regulatory affairs, pharmacovigilance, and scientific/medical writing. Along with delivering high-quality services, Clinforge is establishing its own peer-reviewed journal, the Journal of Drug Development & Clinical Research (JDDCR), to advance academic publishing in pharmaceutical and life sciences. Position: Scientific Writer 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, white papers, and patient education material. Conduct literature reviews and ensure referencing accuracy using tools like EndNote, Mendeley, or Zotero. Collaborate with researchers, clinicians, and regulatory teams to ensure scientific accuracy and compliance. Ensure all documents meet journal-specific and regulatory guidelines (ICMJE, CONSORT, GCP, etc.). Journal Setup & Publication: Support in designing and managing Clinforge’s in-house journal (JDDCR). Assist with editorial workflows, peer review management, and DOI/ISSN processes. Coordinate with editorial board and reviewers to ensure timely publication of issues/volumes. Edit, proofread, and prepare manuscripts for journal volumes, special issues, and conference proceedings. Maintain the highest standards of clarity, accuracy, and integrity in all scientific outputs. Qualifications & SkillsMaster’s or PhD in Life Sciences / Pharmacy / Biotechnology / Clinical Research. Minimum 01 years of experience in scientific or medical writing (exceptional freshers may be considered). Strong command of English language, grammar, and scientific terminology. Prior exposure to journal editorial workflows / publishing platforms will be a strong advantage. Knowledge of regulatory writing (CSR, CTD/eCTD) preferred. Proficiency in reference management and formatting. Excellent time management, communication, and teamwork skills.