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
- Medical Writer in Medical Communications team developing scientific publications for clients in pharmaceutical and healthcare. Involves analysis and clear communication of clinical trial data.
Responsibilities
- You will be based in our Medical Communications team as a Medical Writer, specialising in the strategic planning and development of scientific publications
- Your work will involve the detailed analysis and clear, creative communication of clinical trial data through abstracts, posters, oral presentations and manuscripts
- You will support a range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organisations
Requirements
- A degree level or higher qualification in a scientific discipline (minimum CAP or GPA 4/5 or equivalent)
- An excellent written and spoken fluency in English
- An ability to communicate scientific materials clearly in both written and oral form
- An excellent understanding of and ability to apply scientific concepts
- A close attention to detail
- An aptitude for and experience of scientific writing
- A competency in Microsoft Word, Excel and PowerPoint
- An exceptional level of organisational skills
Benefits
- Hybrid working options
- Generous holiday allowance
- Flexible working hours
- Private medical insurance
- Comprehensive travel insurance
- Full funding for external training
- Regular company-funded social activities
Job title
Job type
Experience level
Salary
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.