Medical Writer
Listed on 2026-02-16
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Healthcare
Clinical Research, Medical Science
As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, Liva Nova is where your talent can truly thrive.
Join our talented team members worldwide to become a pioneer of tomorrow—because at Liva Nova,
we don’t just treat conditions — we aspire to alter the course of lives.
The Medical Writer prepares clinical evaluation plans (CEP) and reports (CER), Post Market Clinical Follow-up (PMCF) Plans and Reports, and performs ad hoc and systematic literature reviews.
Position SummaryPrevious experience in medical writing/reading. Understanding of the impact factor and relevance of scientific journals and papers.
Strong skills in data statistics and study design.
Industry experience that includes the understanding of Clinical Development, Regulatory Affairs and Marketing activities, through different stages. Understanding of the international guidelines, US and European.
Ability to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment. Efficient writing of large documents per project deadlines.
Ability to work well with a diverse group of personalities, team player, flexible and adaptable; ability to build relationships, both internally and externally to the organization.
Excellent English oral and written (C2); excellent oral communication and medical writing skills.
Familiarity with industry-wide good publication practices.
EducationMinimum of Bachelors (4 year university) degree. Graduate degree preferred.
Biomedical or medical or pharmaceutical industry degree is preferred, or a strong expertise in medical device.
ExperienceMinimum of 5 years of other relevant experience in areas such as medical or clinical research activities (eg, clinical trial management support, data management, submission dossier, Clinical Study Reports, etc.)
Willingness to travel: up to 25% of the job may be travel
Welcome to impact. Welcome to innovation. Welcome to your new life.
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