Senior Medical Writer

3 weeks ago


Delhi, India Celegence Full time
Qualification(s)Bachelor’s Degree/Post Graduation in any relevant Life Sciences field. Master’s Degree is preferred.Experience(s)Publication experience in scientific journals preferableMinimum 3 years of experience in Medical Device Regulatory documentationFamiliarity with the Life Sciences Industry, preferably Regulatory ServicesHands on experience on CEP/CER/PMSR/PSUR processExperience in creating high quality deliverables for customersExperience in handling projects and engaging with multiple clients independentlyExperience of working on projects involving all devices classes from various Therapeutic AreasTechnical SkillsKnowledge of clinical evaluation and related documents and regulatory requirementsProficiency in comprehension of scientific data and medical terminology and efficiency in summarizing information from source documents and published literatureProficiency with Microsoft Office (Word, Excel, and Outlook)Hands on experience on presentation tools such as PowerPoint, Visio etc., and referencing tools such as Zotero, Endnote, etc. will be an added advantage.Effective reviewing skills for review of work done by trainees/junior writers.Soft SkillsStrong verbal and written communications skillsAbility to work as part of a team.A constant zeal towards learning and skill developmentPotential to multitask and work within timelines.Ability to understand and deliver on customer requirements.Mentoring skills to act as trainer/mentor for junior members of the teamCompetenciesBasic English grammar, punctuation, and sentence constructionLogical comprehensionKnowledge of medical terminologyExcellent Communication (Writing and Verbal)Quality focused mindsetGood time managementGood stakeholder managementPersonal TraitsPositive Attitude, Initiative and Commitment, Detail Oriented, Team player, Focused and sincere, Ownership and accountability of work.Roles and ResponsibilitiesEnsure on-time development and delivery of various sections of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across therapeutic areasActively engage with internal stakeholders and cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory AffairsDeliver solutions that are customized per client requirements in terms of language, content, format, and presentation.Assist the Team Lead/Manager in the development of schedules to ensure timely delivery.Manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables.Train and mentor junior members of the team on technical/process related aspectsConduct proofreading, editing, document formatting, review comment incorporation and document completion / approval activitiesPerform literature searches on various databases.Screening, appraisal per pre-defined criteria, and summarization of articlesInterpret and present data from device-specific technical documents such as User Manuals/Instructions for UseSummarize quantitative data from post-marketing surveillance.Conduct editing, proofreading, document formatting, and other document completion/approval activities.



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