Position Summary: The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review. The successful candidate has a clear understanding of content requirements for key clinical documents based on regulatory requirements for all phases of development and will complete MW activities with impeccable attention to detail. Essential functions of the job include but are not limited to: Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidance's Ensures smooth and effective document management from start to finish (ie, from template to final, approved version) in collaboration with Sponsor, external vendors, and/or internal Precision project teams/departmentsAbility to independently formulate key messages from clinical study data Ability to author complex content using knowledge/skills and understanding of processesAbility to communicate clearly and concisely both in writing and verbally with internal and client teamsContributes to the development and maintenance of medical writing processes, SOPs, templates, and work instructions for key documentsExcellent problem-solving skillsPerforming literature-based research to support writing activitiesOther duties as assigned Qualifications:



Minimum Required:BS degree or equivalent in a scientific or medical discipline with relevant writing expertise 5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting or 7+ years of experience as a Principal Medical Writer. Other Required: Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint Clear understanding of applicable regulations (eg, ICH, FDA, GCP), clinical trial transparency requirements (ie, EudraCT, CT.gov), and eCTD requirements for all phases of developmentImpeccable attention to detail and ability to complete writing assignments in a timely manner Ability to work effectively in a fast-paced environment with multiple high-priority projects with no instruction on routine work and minimal instruction on new assignments Preferred: Advanced degree (MS/PhD)Oncology and/or rare disease experience (especially protocol and CSR development) #LI-Remote#LI-TB1Any data provided as a part of this application will be stored in accordance with our Privacy Policy. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected] you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

📌 Senior/Principal Medical Writer - Remote Working (España)
🏢 Precision Medicine Group
📍 España