
Senior Medical Information Writer
Share job link
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Senior Medical Information Writer
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 essential 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.
Position Overview:
In this role, you will provide high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients. You will provide technical consultation and advice on strategy, regulations and industry best practices. As a Sr. Medical Information Writer you will demonstrate subject matter and therapeutic area expertise. You’d have to effectively manage medical writing projects to deliver quality products in agreed timelines. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
Essential Duties and Responsibilities (other duties may be assigned):
Ability to effectively manage medical writing projects to deliver quality products in agreed timelines by demonstrating subject matter and therapeutic area expertise.
Collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
Independently researches, writes, and edits standard medical information writing deliverables across various therapeutic areas. Independently writes more complex medical writing deliverables. Examples may include global or regional standard response documents, custom responses, and FAQs. Provides senior review of documents and training/mentoring for other writers.
Manages all aspects of planning, organizing, and executing projects without supervision, including: developing project timelines, standards, budgets, forecasts and contract modifications. Liaises with other functional units as necessary. Identifies and escalates out-of-scope project activities in a timely manner and proposes solutions.
May manage several long-term projects concurrently.
Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
Interacts with internal and external personnel on significant matters often requiring coordination between functional areas. Networks with senior internal and external personnel in own area of expertise.
Normally receives little instruction on day-to-day work, general instructions on new assignments. Demonstrates good judgment in selecting methods and techniques for obtaining solutions.
Represents the department as a prime contact on projects including Project Launch Meetings, Review meetings, client audits, bid defenses, and capabilities presentations. Establishes and develops client relationships; independently initiates and leads interactions with clients. Assists with business development and development of budgets and proposals.
Education, Professional Skills & Experience:
Previous experience in Medical Information Writing is essential
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years’) or equivalent combination of education, training, & experience.
Experience working in the pharmaceutical/CRO industry preferred.
Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.
Personal Skills & Competencies:
Aptitude to accurately work with, manipulate and format numbers, numerical information, and data of various types to provide evidence, information and insights.
Demonstrated ability to communicate and document information effectively in written English, including the ability to produce reports, documents, emails and other written pieces which are well-organized, free from errors and are appropriately adjusted to the characteristics and needs of the audience.
Able to analyze complex issues and evidence, identify cause-effect relationships and generate effective solutions.
Able to create, communicate and manage effective project plans that support the delivery of overall project objective(s); to identify, manage and guide project team members; to monitor and report on progress in an organized fashion; and to deliver the required results.
Demonstrates sound professional judgment in analyzing, responding to, and resolving enquiries, issues and escalations.
Able to facilitate the resolution of conflict among team members and clients, through listening and understanding the cause(s), gaining agreement on an appropriate course of action, and following up to ensure a successful outcome.
Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook).

類似した求人の通知を受け取る
成功!
成功!類似した求人に登録しました
失敗!

あなたの興味に基づいて、カスタマイズされた仕事の推奨事項を取得します。

プロフィールに基づいた求人候補
類似の仕事
-
Senior / Project Coordinator - Data Analysis and Compliance, client dedicated
ロケーション Ware, ハートフォードシャー州, 英国 求人ID R-01286873
Hands-on support as required including tracking, migrating and verifying data and documents between various repositories (internal and/or external). Responsible for scheduling and planning their own w...
-
(Senior) Medical Director - Rheumatology (Client - dedicated), EMEA
求人ID R-01291460
Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and ap...
-
Medical Affair Statistician Specialist
ロケーション Remote, 英国 求人ID R-01308138
This role offers the opportunity to collaborate with Senior Statisticians and contribute to the preparation of statistical analysis plans, develop analytical datasets, write programs to execute statis...
-
Executive Oncology Epidemiology Researcher, Evidera
求人ID R-01301029
The Senior Research Scientist / Epidemiologist acts as the independent principal investigator (PI) of projects responsible for overseeing all aspects of delivery of retrospective and/or hybrid studies...
-
Senior Medical Project Coordinator, EMEA
求人ID R-01307151
Independently functions as the Project Lead for medical monitoring services when SAE case processing has not been contracted. Previous experience that provides the knowledge, skills, and abilities to...
-
Research Scientist/Senior Research Scientist - Patient Centered Research
ロケーション Remote, 英国 求人ID R-01302814
The ITR Senior Research Scientist is the independent Principal Investigator of projects responsible for supervising all aspects of project delivery; delegates project management tasks to more junior s...
-
Clinical Data Strategist
求人ID R-01310955
The CDS acts as the lead subject matter expert and interdepartmental and client liaison for data review activities with focus on the development of study level analytic tools to detect, investigate, d...
-
Executive Epidemiology Researcher - Safety Outcomes, Evidera
求人ID R-01301021
The Senior Research Scientist / Epidemiologist acts as the independent principal investigator (PI) of projects responsible for overseeing all aspects of delivery of retrospective and/or hybrid studies...
-
Snr eCOA/eConsent Project Manager
ロケーション Remote, 英国 求人ID R-01310948
In this role, you will help revolutionise patient care through innovative digital technologies, making a real-world impact and gaining valuable career skills. Works with major functional area leads to...
求職者も閲覧