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.
Responsibilities
You will be based in the Medical Communications team as a Medical Writer
Specialising in the strategic planning and development of scientific publications
Involve in the detailed analysis and clear communication of clinical trial data
Collaborate with clients and internal teams on projects
Deliver high quality scientific materials for submission to journals and conferences
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
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.
Medical Writer at Real Chemistry developing scientific copy for healthcare communications. Collaborating with medical writers and adhering to style guidelines for various projects.