Medical Writer
We are Reckitt
About the role
The role of Medical Writer is integrated within Global Medical Science and reports directly to the Medical Writing Manager. This is a crucial role, requiring the successful applicant to take responsibility for writing, editing and maintaining high quality Medical and Clinical documentation for Regulatory submissions, which is essential for business growth and building a strong reputation with Health Authorities, as well as facilitating and supporting the on-going marketing of Reckitt medical devices, cosmetics, medicines and general products.
The Medical Writer will research, create and revise various documents associated with clinical research. Working closely alongside team members, the Medical Writer will ensure that all written documentation meets the strategic objectives and is produced to the highest possible scientific and editorial standards.
Your responsibilities
- Manage the writing, editing and reviewing of diverse Regulatory and Clinical Documents. These include but are not limited to: briefing documents, investigators’ brochures, clinical evaluation reports (CERs) and other Medical/Regulatory documents
- Provide input and edit/review of Regulatory and Clinical documents, as required, across all Reckitt product classifications, i.e. medical devices, cosmetics and medicines
- Manage the quality, accuracy and compliance with internal and external standards and the timely production of English and Mandarin language documents using electronic document management system
- Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation
- Develop, implement and manage templates for the standardisation of Regulatory and Clinical Documentation to support development and registration activities
- Develop an understanding of the regulatory landscape and documentation requirements for Medical Device registration in China
- Coordinate and conduct interdepartmental team review and sign-off of document deliverables according to guidelines/SOP’s including: distribution of drafts, chairing review meetings, incorporating revisions and completing sign off procedures
- Coordinate and collate high quality responses to Regulatory questions that arise during dossier/technical file review as required
- Review, improve and maintain existing documentation and create and maintain audit system/trails of all document changes and respond to Medical Information requests
The experience we're looking for
- Bachelor’s degree preferably healthcare or life sciences (or equivalent)
- Experience in preparing medical or scientific documents to a high standard is essential. Experience of working in or for the Healthcare OTC industry, and/or direct experience of drafting documentation to international Regulatory standards is desirable
- Ability to understand complex clinical documentation and to critically appraise internal and external data for accuracy and robustness Demonstrated knowledge of Medical Device/drug development processes and understanding of healthcare compliance laws and guidelines is desirable
What we offer
Equality
Job Segment:
Medical Device, Medical Research, Clinical Research, Counseling, Medical, Healthcare