Staff Medical Writer

Work Flexibility: Hybrid<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p><b>What will you do:</b></p><ul><li>Conduct systematic literature searches using scientific databases and search tools.</li><li>Critically analyze and summarize clinical data from published literature and other scientific sources.</li><li>Develop literature search protocols, screening strategies, and documentation.</li><li>Maintain strong working knowledge of global medical device approval pathways, with emphasis on EU MDR and European regulatory frameworks.</li><li>Demonstrate thorough understanding of Good Clinical Practice (GCP), applicable standards, and industry practices.</li><li>Maintain professional expertise by regularly reviewing clinical literature and contributing in cross-functional project meetings.</li><li>Understanding of Clinical Study related documents.</li></ul><p></p><p><b>What you need: </b></p><p></p><p><b>Basic Qualifications:</b></p><ul><li>Postgraduate degree/Master’s in allied paramedical fields (Pharmacy, Biotechnology, Biomedical Engineering etc.)</li><li>Minimum 5&#43; years of experience in delivering high-quality scientific and clinical writing with attention to detail.</li><li>Expertise in scientific literature databases such as:PubMed, Embase, Google Scholar, ProQuest, Cochrane etc.</li><li>Understanding of medical device technologies, classifications, and clinical applications.</li><li>Strong understanding of medical device regulations (knowledge in EU MDR, ISO 14971), clinical evaluation, risk-benefit analysis.</li><li>Ability to work in collaboration with cross-functional teams including:<br />R&amp;D, Regulatory Affairs, Clinical Affairs, Clinical Safety, Biostatistics, Data Management, Product Management, and external stakeholders.</li><li>Well verse with MS Office / MS Word</li><li>Excellent communication and presentation skills</li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li>PhD in allied health sciences with 4–6 years of experience</li><li>Experience in using tools such as: Distiller, Readcube, Endnote, Power BI etc.</li><li>Good analytical and problem-solving skills</li><li>Ability to work with minimal supervision, managing multiple deliverables, and ensuring compliance with applicable global regulatory and quality standards</li><li>Strong accountability and ownership to ensure deliverables meet timelines and compliance requirements.</li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Travel Percentage: None<p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p></p><p></p><p></p><p></p>