Writer, Medical Information - Evidera At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital, and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Location/Division Specific Information: Effective communication of evidence and information is crucial to conveying the value of products. With approximately 20 years of experience, our highly trained staff provide medical writing services for the peri- and post-approval phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standard processes, and corporate guidance.
Discover Impactful Work:
A day in the Life: Independently researches, writes, and edits standard medical information writing deliverables (global or regional standard response documents, custom responses, and FAQs) across various therapeutic areas; may also independently write, or assist with more complex medical writing deliverables.Participates in developing project timelines, standards, budgets, forecasts, and contract modifications. 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 a variety of factors.Develops professional expertise and applies company policies and procedures to resolve a variety of issues.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. Keys to Success:
Education and Experience: Bachelor's degree in a scientific field or equivalent and relevant formal academic/vocational qualification.Proven experience as a Medical Information Writer that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).Experience working in the pharmaceutical/CRO industry 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 drug development process.Good computer skills and skilled with client templates. Knowledge, Skills, Abilities: Effective administrative, organizational and planning skills; attention to detail and quality.Ability to work on own initiative and effectively within a team.Effective oral and written communication skills.Great judgment and decision-making skills. Physical Requirements / Work Environment: Normal and routine office duties.Domestic and international travel may be required. Benefits: We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
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