Social network you want to login/join with:
Medical Writer - Medical Information
Client:
Thermo Fisher Scientific
Location:
United Kingdom
Job Category:
Medical Writing
EU work permit required:
Yes
Job Reference:
0a341219256a
Job Views:
77
Posted:
13.02.2025
Expiry Date:
30.03.2025
Job Description:
1. 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 may include global or regional standard response documents, custom responses, and FAQs.
2. Participates in developing project timelines, standards, budgets, forecasts, and contract modifications.
3. Assists in the management of project budget and forecast.
4. Contributes to developing contract modifications with oversight.
5. May represent Medical Writing in bid defenses and capabilities presentations.
6. Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.
7. Develops professional expertise and applies company policies and procedures to resolve a variety of issues.
8. Normally receives general instructions on routine work, and more detailed instructions on new projects or assignments. Exercises judgment within defined procedures and practices to determine appropriate action.
9. Contacts are primarily internal to the company, but may have frequent external customer/vendor contacts on routine matters. Builds productive internal/external working relationships.
Education, Professional Skills & Experience:
1. Bachelor's degree in a scientific discipline or equivalent and relevant formal academic/vocational qualification.
2. Previous experience as a Medical Information Writer that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’) or equivalent combination of education, training, & experience.
3. Experience working in the pharmaceutical/CRO industry preferred.
4. Solid medical writing skills, including grammatical, editorial, and proofreading skills.
5. Ability to interpret and present complex data accurately and concisely.
6. Good knowledge of regulatory documentation and drug development process.
7. Good computer skills and skilled with client templates.
8. Good knowledge of document management systems and other relevant applications (Word, Excel, Outlook).
Personal Skills & Competencies:
1. Effective administrative, organizational and planning skills; attention to detail and quality.
2. Ability to work on own initiative and effectively within a team.
3. Effective oral and written communication skills.
4. Great judgment and decision-making skills.
#J-18808-Ljbffr