Senior Medical Writer – Italy (Home-based in Sienna)
Clintec is actively recruiting for a Senior Medical Writer to join our expanding global company in Italy. This is a home-based opportunity working in Sienna. By working for Clintec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.
Medical Writer is responsible for writing, reviewing and editing medical writing documents including but not limited to regulatory and medical communication deliverables under the guidance of medical writing managers and directors. In addition, the Medial Writer shall co-ordinate medical writing activities between the internal team and client, ensuring projects are completed on or ahead of time and on budget, according to the applicable SOPs.
Responsibilities of the Senior Medical Writer:
Medical writing of all types of regulatory and clinical study documentation including Investigators' Brochures, CTD modules – summary and overviews, clinical study reports and protocols
Author documents per client specifications, templates, style guides, and other guidance documents
Provide clinical review for patient narratives and other documents
Act as a client point of contact
Maintain collaborative, proactive, and effective communication with both client and internal teams
Participate in project-related meetings and teleconferences
Previous medical or scientific writing experience – 3 to 5 years of prior related experience
Experience in vaccines and immunology would be an added advantage
Strong computer skills, including proficiency with Microsoft Outlook, Word, Excel, and PowerPoint
Ability to analyse and summarise data from a diverse range of indications
Advanced scientific writing skills
Post-graduate science degree in a biomedical field
Fluency in written and spoken English and Italian languages
Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 50 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.
Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package