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Medical Writer - Medical Information, United Kingdom
Client: Thermo Fisher Scientific
Location: United Kingdom
Job Category: -
EU work permit required: Yes
Job Reference: 0a341219256a
Job Views: 3
Posted: 05.05.2025
Expiry Date: 19.06.2025
Job Description:
(other duties may be assigned):
- Independently researches, writes, and edits standard medical information writing deliverables across various therapeutic areas; may also independently write, or assist with more complex medical writing deliverables. Examples include global or regional standard response documents, custom responses, and FAQs.
- Participates in developing project timelines, standards, budgets, forecasts, and contract modifications.
- Assists in the management of project budget and forecast.
- Contributes to developing contract modifications with oversight.
- May represent Medical Writing in bid defenses and capabilities presentations.
- Works on problems of moderate scope where analysis of situations or data requires a review of various factors.
- Develops professional expertise and applies company policies and procedures to resolve issues.
- Receives general instructions on routine work, and detailed instructions on new projects or assignments. Exercises judgment within defined procedures and practices to determine appropriate action.
- Contacts are primarily internal to the company, but may include external customer/vendor contacts on routine matters. Builds productive internal/external relationships.
Education, Professional Skills & Experience:
- Bachelor's degree in a scientific discipline or equivalent with relevant academic/vocational qualification.
- Previous experience as a Medical Information Writer providing the knowledge, skills, and abilities to perform the job (comparable to 2+ years) or an equivalent combination of education, training, & experience.
- Experience working in the pharmaceutical/CRO industry is preferred.
- Solid medical writing skills, including grammatical, editorial, and proofreading skills.
- Ability to interpret and present complex data accurately and concisely.
- Good knowledge of regulatory documentation and the drug development process.
- Proficient with computer skills, including client templates, document management systems, and relevant applications (Word, Excel, Outlook).
Personal Skills & Competencies:
- Effective administrative, organizational, and planning skills; attention to detail and quality.
- Ability to work independently and effectively within a team.
- Excellent oral and written communication skills.
- Good judgment and decision-making skills.