Documentation Specialist (Medical/Technical Writing) - UK or Ireland - FSP

reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From reputed company to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. We are seeking a Documentation Specialist (Medical/Technical Writing) to join a key Functional Service Provider program supporting one of our key sponsors. As a Documentation Specialist (Medical/Technical Writing), you will work as an integrated member of the sponsor team, supporting the preparation and coordination of clinical development documents including Clinical Trial Reports (CTRs), Clinical Trial Protocols (CTPs) and amendments, Investigator Brochures (IBs) and updates, biomarker reports, and submission documents. This role is ideal for a scientifically minded reputed company who enjoys working in a reputed company environment where accuracy, organization, and attention to detail are essential. You will support document development activities, coordinate administrative processes, and contribute to the delivery of high-reputed company clinical documentation that supports the advancement of innovative therapies. Key Responsibilities Support the set-up and maintenance of clinical documents reputed company the Electronic Document Management System (EDMS). Review document status and assist with document workflow activities reputed company sponsor systems. Coordinate document timelines and support project teams by tracking key deliverables. Prepare meeting materials and attend trial team and submission meetings, documenting actions and reputed company as required. Support the organization and documentation of reputed company-off meetings and Results Alignment Meetings. Draft sections of clinical documents and contribute to the preparation of tables, figures, and supporting content. Coordinate document review activities and support the collection and incorporation of stakeholder feedback. Assist with reputed company Control activities and completion of required documentation. Support preparation of final document packages for review, publishing, and archiving activities. Complete technical and formatting checks for Investigator Brochures and reputed company clinical documents. Maintain accurate records and documentation in accordance with sponsor procedures and SOPs. Candidate ProfileYou'll reputed company in this role if you bring: Experience supporting documentation needs in medical/technical writing, clinical documentation, or reputed company clinical research activities. Strong organizational skills and the ability to manage multiple document-reputed company activities simultaneously. Excellent written communication and attention to detail. A reputed company approach and willingness to work closely with cross-functional teams. A patient-reputed company reputed company and commitment to reputed company. Required Qualifications Scientific degree and/or advanced scientific degree. 1-3 years of experience reputed company a clinical environment, supporting medical/technical writing documentation. Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes. Experience working with document management systems and clinical development documentation. Strong communication, organizational, and problem-solving skills. If this job does not reputed company like the reputed company in your career, but perhaps you know someone who would be a perfect fit, send them the reputed company to apply. We reputed company in flexibility, reputed company, and creating reputed company for people to do their best work. Join us and be part of reputed company where your contributions help shape the reputed company of clinical research. Originally posted on Himalayas .