Medical Writer

Medical Writer

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Create clinical evaluation plans and reports while collaborating with diverse teams.
  • Company: LivaNova is a leading medical equipment manufacturer focused on improving lives.
  • Benefits: Enjoy a full-time role with opportunities for travel and professional growth.
  • Why this job: Make a real impact in healthcare while developing your writing and research skills.
  • Qualifications: Requires a Bachelor's degree and 5 years of relevant experience in medical writing.
  • Other info: LivaNova values diversity and promotes a fair recruitment process.

The predicted salary is between 36000 - 60000 £ per year.

LivaNova Gloucestershire, England, United Kingdom

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LivaNova Gloucestershire, England, United Kingdom

Join to apply for the Medical Writer role at LivaNova

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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

LivaNova is an exceptional employer located in Gloucestershire, offering a dynamic work culture that fosters collaboration and innovation in the medical equipment manufacturing sector. Employees benefit from comprehensive professional development opportunities, a commitment to diversity and inclusion, and the chance to make a meaningful impact on patients' lives through their work. With a focus on employee well-being and a supportive environment, LivaNova stands out as a rewarding place to advance your career as a Medical Writer.
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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 clinical evaluation plans and reports in the medical device industry. This will not only enhance your understanding but also demonstrate your commitment to staying updated, which is crucial for a Medical Writer role.

✨Tip Number 2

Network with professionals in the medical writing field, especially those who have experience with clinical evaluations and regulatory affairs. Engaging in discussions or attending relevant conferences can provide insights and potentially lead to referrals.

✨Tip Number 3

Showcase your ability to manage multiple projects by discussing any relevant experiences where you successfully juggled various tasks. This skill is essential for the fast-paced environment at LivaNova, and highlighting it can set you apart.

✨Tip Number 4

Prepare to discuss your familiarity with good publication practices and how they apply to your previous work. Being able to articulate this knowledge during interviews will demonstrate your readiness for the responsibilities of a Medical Writer.

We think you need these skills to ace Medical Writer

Medical Writing
Clinical Evaluation Plans (CEP)
Clinical Evaluation Reports (CER)
Post Market Clinical Follow-up (PMCF) Plans and Reports
Systematic Literature Reviews
Data Statistics
Study Design
Regulatory Affairs Knowledge
Excellent English Oral and Written Communication
Project Management
Cross-Functional Collaboration
Good Publication Practices
Ability to Manage Multiple Projects
Adaptability and Flexibility
Strong Interpersonal Skills

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities of a Medical Writer at LivaNova. Familiarise yourself with clinical evaluation plans, literature reviews, and the specific requirements mentioned in the job description.

Tailor Your CV: Highlight your relevant experience in medical writing, clinical research, and any familiarity with regulatory affairs. Make sure to emphasise your skills in data statistics and study design, as these are crucial for the role.

Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for the medical field and your understanding of the impact of your work. Mention specific projects or experiences that align with the job requirements, demonstrating how you can contribute to LivaNova's mission.

Proofread Your Application: Ensure that your application is free from grammatical errors and typos. Given the importance of excellent written communication in this role, a polished application will reflect your attention to detail and professionalism.

How to prepare for a job interview at LivaNova

✨Showcase Your Medical Writing Experience

Be prepared to discuss your previous experience in medical writing, particularly any clinical evaluation plans or reports you've worked on. Highlight specific projects where you collaborated with cross-functional teams and how you managed timelines.

✨Demonstrate Your Understanding of Scientific Literature

Since the role involves performing literature reviews, be ready to talk about your familiarity with scientific journals and how you assess the impact factor of publications. You might even want to mention a recent study that caught your attention.

✨Emphasise Your Communication Skills

Excellent oral and written communication skills are crucial for this position. Prepare examples of how you've effectively communicated complex information to diverse audiences, whether through presentations, reports, or team collaborations.

✨Prepare for Questions on Regulatory Guidelines

Understanding international guidelines is key for this role. Brush up on US and European regulations related to medical writing and be ready to discuss how you've applied these in your past work.

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