Medical Writer in Costello Medical's Medical Communications team specializing in scientific publications and communication of clinical trial data. Collaborating with clients to deliver high - quality scientific materials.
About the role
- Senior Medical Writer at Avalere Health producing editorial content to support healthcare communication goals. Collaborating with teams to deliver quality projects on time and within budget.
Responsibilities
- developing and delivering original, accurate, high-quality content (manuscripts, slides, and other editorial assignments) within the project specifications, timeline, and budget
- providing high‑quality editorial oversight for both project work and business development efforts
- striving to function as a scientific and therapeutic expert (within limitations of budget and timelines) for assigned project teams
- functioning as the primary writer for assigned accounts
Requirements
- Bachelor’s degree in the life sciences; PharmD or PhD highly preferred
- Ideally 2+ years' of medical writing experience, preferably MedAffairs
- Proficiency in the use of MS Office, specifically Word, PowerPoint, and Excel
- Proficiency in Internet and PubMed searches
- Ability to work independently with minimal supervision, and as part of a team
Benefits
- up to a 7% pension contribution
- life insurance
- income protection
- private medical insurance
- flexible working arrangements
- option to work from anywhere across the globe two weeks each year
- 25 days of annual leave plus two personal well-being days
- gifted end-of-year holidays
- early Summer Friday finish in June, July, and August
- free counselling through employee assistance program
- personalized health support
- enhanced maternity, paternity, family leave, and fertility policies
- continuous opportunities to professionally develop with on-demand training, support, and global mobility opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
RN specializing in clinical documentation integrity for pediatric patients at Connecticut Children's. Collaborating with healthcare providers to enhance documentation standards and accuracy.
Principal Medical Writer at IQVIA producing inspection - ready Clinical Study Reports for Phase 1 studies. Collaborating with teams to ensure compliance with regulatory and internal guidelines while maintaining document quality.
Principal Digital Medical Writer translating complex scientific evidence into engaging medical communications. Leading evidence synthesis projects and collaborating with digital, data, and design teams in a hybrid role.
Medical Writer creating and reviewing regulatory and public - facing documents. Supporting clinical and regulatory strategies with an emphasis on compliance and health literacy principles.
Senior Medical Writer overseeing high - quality clinical and regulatory documents at Ipsen, a biopharmaceutical company. Leading cross - functional teams and contributing to regulatory strategy while ensuring compliance and innovation in medical writing practices.
Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.
Medical Copywriter creating pharmaceutical promotional content for a global digital agency. Developing strategies and overseeing editorial quality for marketing communications in the life sciences sector.
CDI Nurse assisting GBMC Health Partners with documentation improvement efforts. Collaborating with physicians and clinicians on patient records and risk management.
Clinical Documentation Specialist working with healthcare teams to ensure accurate medical record documentation. Aiding in compliance and coding education for clinical documentation improvement.