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- Tasks: Prepare clinical evaluation plans and reports, conduct literature reviews, and collaborate with teams.
- Company: Join LivaNova, a leader in medical technology dedicated to improving lives.
- Benefits: Enjoy flexible working options, travel opportunities, and a diverse, inclusive workplace.
- Why this job: Make a real impact in healthcare while developing your writing and research skills.
- Qualifications: Bachelor's degree required; 5 years of relevant experience in medical writing or clinical research.
- Other info: LivaNova values diversity and promotes a fair recruitment process.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Join to apply for the Medical Writer role at LivaNova
Join to apply for the Medical Writer role at LivaNova
Join us today and make a difference in people\’s 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 Summary
- Ensure completion of clinical evaluation plans (CEP) and reports (CER) and Post Market Clinical Follow-up (PMCF) Plans and Reports per each product family within the Cardiac Surgery (CS) franchise in cooperation with all main internal and external stakeholders within the agreed timelines.
- Perform ad hoc and systematic literature reviews on global scientific newly released data to support Product Market Surveillance reports, Global Signal Detection meetings, Study Design Protocols, Global Market Value Dossiers, Regulatory Dossiers, Medical Affairs scientific summary documents.
- Provide writing skills to protocols and clinical study reports and all relevant clinical documentation (literature review plans/reports; study protocols/reports; scientific manuscript; congress abstracts/posters/presentations).
- Collaborate with cross-functional teams to develop clinical evaluation strategies.
Knowledge, Skills And Abilities Required
Previous 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.
Education
Minimum 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.
Experience
Minimum 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
Valuing Different Backgrounds
LivaNova values equality and diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination. Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice To Third Party Agencies
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware Of Job Scams
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for “See Open Jobs” on https://www.livanova.com/en-us/careers, and check that all recruitment emails come from an @livanova.com email address.
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Marketing, Public Relations, and Writing/Editing
-
Industries
Medical Equipment Manufacturing
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Medical Writer employer: LivaNova
Contact Detail:
LivaNova Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer
✨Tip Number 1
Familiarise yourself with the latest trends and guidelines in medical writing, especially those related to clinical evaluation plans and reports. This knowledge will not only enhance your understanding but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the medical writing community, particularly those who have experience in cardiac surgery or related fields. Engaging with industry experts can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences in managing multiple projects and how you prioritised tasks under tight deadlines. Being able to articulate your project management skills will be crucial during interviews.
✨Tip Number 4
Showcase your ability to collaborate with cross-functional teams by preparing examples of past teamwork experiences. Highlighting your adaptability and relationship-building skills will resonate well with the hiring team.
We think you need these skills to ace Medical Writer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in medical writing, clinical research, and any specific projects that align with the responsibilities outlined in the job description. Use keywords from the job posting to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical writing and your understanding of clinical evaluation plans and reports. Mention specific experiences that relate to the job requirements and how you can contribute to the team.
Showcase Your Writing Skills: Include samples of your previous medical writing work, such as clinical study reports or literature reviews, if possible. This will give the hiring team a clear idea of your writing style and expertise.
Highlight Relevant Education and Experience: Clearly state your educational background, especially if you have a degree in biomedical, medical, or pharmaceutical fields. Emphasise your years of experience in medical writing and any familiarity with regulatory guidelines, as these are crucial for the role.
How to prepare for a job interview at LivaNova
✨Showcase Your Medical Writing Experience
Be prepared to discuss your previous experience in medical writing. Highlight specific projects where you prepared clinical evaluation plans or reports, and explain how your contributions made a difference.
✨Demonstrate Knowledge of Scientific Literature
Familiarise yourself with recent scientific publications relevant to the cardiac surgery field. Be ready to discuss how you approach literature reviews and how you stay updated on new data that impacts product market surveillance.
✨Emphasise Collaboration Skills
Since the role involves working with cross-functional teams, be sure to provide examples of how you've successfully collaborated with diverse groups. Discuss any challenges you faced and how you overcame them to achieve project goals.
✨Prepare for Technical Questions
Expect questions related to clinical development, regulatory affairs, and study design. Brush up on your understanding of international guidelines and be ready to discuss how these impact your writing and project management.
