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- Tasks: Write and edit regulatory and clinical documents for medical devices.
- Company: Join a leading innovator in the medical device industry focused on improving patient outcomes.
- Benefits: Enjoy a 6-month contract with potential for growth and valuable experience.
- Why this job: Be part of a mission-driven team that values scientific research and innovation.
- Qualifications: Bachelor's degree in a scientific field; experience in medical writing is essential.
- Other info: Must have UK passport or visa; remote work options may be available.
The predicted salary is between 36000 - 60000 £ per year.
Your new company My client, a leading innovator in the medical device industry, dedicated to improving patient outcomes through cutting-edge technology and rigorous scientific research, is looking for a talented and detail-oriented Regulatory /Clinical Medical Writer to join their team for a 6-month initial contract.Your new role As the Regulatory/ Clinical Medical Writer, you will be involved in the development, writing and editing of regulatory and clinical documents such as protocols, Clinical Study reports, regulatory submissions and Investigator brochures. You will conduct literature reviews and summarise findings to support clinical and regulatory documents and participate in project meetings and provide input on document strategy and content.What you\’ll need to succeed In order to apply for the Medical Writer contract, you must possess: – Bachelor\’s degree in a scientific discipline; advanced degree is preferred- MUST HAVE significant experience in writing regulatory and clinical documents such as protocols, CSRs, IB, regulatory submissions, in the medical device or pharmaceutical industry- Strong understanding of clinical research and regulatory requirements for medical devices- Excellent writing, editing, and proofreading skills, with keen attention to detail.- Ability to work independently and manage multiple projects with tight deadlines.- Proficiency in Microsoft Office Suite and familiarity with document management systems.- Strong communication and interpersonal skills.- Experience with regulatory submissions (e.g., FDA, EMA, MHRA).- Certification from the American Medical Writers Association (AMWA), European Medical Writers Association (EMWA) or similar organisation.What you need to do now Please submit your resume, cover letter, and writing samples.Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK.To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on 0333 010 6292.Desired Skills and ExperienceMedical Writing
Medical Writer - Clinical / Regulatory employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer - Clinical / Regulatory
✨Tip Number 1
Familiarise yourself with the specific regulatory requirements for medical devices in the UK, especially those related to the FDA, EMA, and MHRA. This knowledge will not only help you in interviews but also demonstrate your commitment to understanding the industry.
✨Tip Number 2
Network with professionals in the medical writing field, particularly those who have experience in regulatory submissions. Attend relevant conferences or webinars to make connections and gain insights that could give you an edge in your application.
✨Tip Number 3
Prepare to discuss your previous writing experiences in detail, focusing on specific projects where you contributed to regulatory documents. Be ready to explain your role, the challenges you faced, and how you overcame them.
✨Tip Number 4
Showcase your attention to detail by being meticulous in your communication during the application process. Whether it's responding to emails or preparing for interviews, clear and precise communication reflects the skills required for a Medical Writer.
We think you need these skills to ace Medical Writer - Clinical / Regulatory
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in writing regulatory and clinical documents. Emphasise your familiarity with protocols, Clinical Study Reports, and regulatory submissions specific to the medical device or pharmaceutical industry.
Craft a Compelling Cover Letter: In your cover letter, express your passion for improving patient outcomes through medical writing. Mention your understanding of clinical research and regulatory requirements, and how your skills align with the company's mission.
Include Writing Samples: Provide writing samples that showcase your ability to create clear and concise regulatory documents. Choose examples that demonstrate your attention to detail and proficiency in the required formats.
Highlight Relevant Certifications: If you have certifications from organisations like the American Medical Writers Association (AMWA) or European Medical Writers Association (EMWA), make sure to mention them prominently in your application. This can set you apart from other candidates.
How to prepare for a job interview at LinkedIn
✨Showcase Your Writing Skills
As a Medical Writer, your writing skills are paramount. Bring along samples of your previous work, especially regulatory and clinical documents, to demonstrate your expertise and attention to detail.
✨Understand Regulatory Requirements
Familiarise yourself with the specific regulatory requirements for medical devices in the UK, such as those from the FDA, EMA, and MHRA. Being able to discuss these during the interview will show your depth of knowledge and commitment to the role.
✨Prepare for Technical Questions
Expect questions related to clinical research methodologies and document strategies. Brush up on your understanding of clinical study protocols and reports, as well as how to conduct literature reviews effectively.
✨Demonstrate Project Management Skills
Since the role involves managing multiple projects with tight deadlines, be ready to discuss your experience in prioritising tasks and managing time effectively. Share examples of how you've successfully handled similar situations in the past.