LivaNova

About the Company

LivaNova PLC is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. Our advanced technologies and breakthrough treatments provide meaningful solutions for the benefit of patients, healthcare professionals and healthcare systems.

At LivaNova, we understand the importance of bringing both clinical and economic value to our customers. We are a strong, market-leading medical technology and services company, offering a diverse product portfolio and global reach. LivaNova is listed on the NASDAQ stock exchange under the ticker symbol “LIVN.”

LivaNova has approximately 2,900 employees worldwide. We are headquartered in London (UK) and maintain a presence in more than 100 countries.

LivaNova is a worldwide leader in cardiopulmonary and neuromodulation, dedicated to creating meaningful products and therapies that transform lives each and every day.

Listed Jobs

Company Name

LivaNova

Job Title

Medical Writer

Job Description

Job Title Medical Writer Role Summary Generate and manage clinical evaluation plans (CEP), clinical evaluation reports (CER), Post‑Market Clinical Follow‑Up (PMCF) plans, and systematic literature reviews. Support product dossiers, protocols, and scientific communication across cross‑functional teams within the Cardiac Surgery franchise. Expectations * Deliver all documentation within agreed timelines. * Maintain high scientific and regulatory accuracy. * Adapt to evolving project priorities and stakeholder needs. * Travel up to 25% of the time as required. Key Responsibilities * Prepare CEPs, CERs, and PMCF plans for each product family. * Conduct ad‑hoc and systematic literature reviews on current scientific data. * Draft protocols, study reports, manuscript sections, abstracts, posters, and presentations. * Contribute to market surveillance, signal detection meetings, and regulatory dossiers. * Collaborate with Clinical Development, Regulatory, and Marketing teams to shape clinical strategies. Required Skills * Proven medical writing experience with journal‑impact knowledge. * Strong statistical and study design competencies. * Understanding of clinical development, regulatory, and marketing workflows. * Familiarity with international guidelines (US, EU) and Good Publication Practice (GPP). * Excellent English (C2 level) oral and written communication. * Ability to manage multiple projects, prioritize tasks, and work effectively in a fast‑paced environment. * Team‑orientated, flexible, and capable of building internal and external relationships. Required Education & Certifications * Minimum Bachelor’s degree (4 years). * Preferred graduate degree or background in Biomedical, Medical, Pharmaceutical, or Medical Device. * No mandatory certifications, though GPP familiarity is advantageous.

Gloucestershire, Belgium

On site

Mid level

05-03-2026