Senior Medical Writer
Senior Medical Writer
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Job Description
About TFS HealthScience
TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full servicecapabilities resourcing and functional service (FSP) solutions.
About the role
The Medical Writer / Technical reviewer will be responsible for the scientific accuracy data and referencing quality appropriate style and correct branding of scientific/medical assets for the sponsor globally. Also will work in an international and crossfunctional environment following global and local guidelines and working closely with internal and external stakeholders to ensure the highest quality for the sponsor assets and gathering data on asset quality and agency performance.
Key Responsibilities
Perform data/referencing quality check of scientific/medical assets; ensuring all content is scientifically accurate and appropriately supported by the Reference Documents.
Review content and identify any noncompliances with the local regulatory guides.
Perform some actions in the Review and Approval platform (Veeva Vault) such as reference tagging or claims object creation.
Check anchors/links to references required to support the scientific/medical assets.
Identify assets that may require prealignment with internal stakeholders.
Flag claims that may be difficult to substantiate or do not follow regulatory/internal guidelines.
Track asset quality data for internal and external reporting.
Qualifications
Experienced Medical Writer or Medical Content Reviewer (35 years) with a scientific background and degree (PharmD MD PhD or Masters) at least 3 years producing or reviewing content for the Pharma/Biotech industry.
Excellent medical writing skills.
Strong attention to detail and accuracy ability to manage and prioritize multiple detailed activities resultsorientated with fast and focused execution.
Good communication coordination and time management skills.
Fluent in oral and written English AND one or more of these languages: German French
Ability to work within a team or across multiple teams (including remotely) as well as independently.
Values teamwork and collaboration diversity and inclusion and innovation.
Prior experience working in content creation for Biotech/Pharma would be advantageous.
Prior experience working in any of the therapeutic areas: Metabolism Cardiovascular Diseases Chronic Kidney Disease Respiratory Inflammation; would be advantageous
Prior experience with the Pharmaceutical Content Review process and/or Veeva Vault would be advantageous.
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients
A Bit More About Us
Our journey began over 27 years ago in Sweden in the city of Lund. As a fullservice global Contract Research Organization (CRO) we build solutiondriven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability are our guiding light serving as the framework for decisionmaking at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
Employment Type
Full Time
