At a Glance
- Tasks: Write and edit clinical documents, ensuring scientific accuracy and regulatory compliance.
- Company: Join an award-winning CRO known for its supportive and innovative culture.
- Benefits: Enjoy remote work flexibility, competitive salary, and a focus on career growth.
- Other info: Be part of a Great Place to Work certified organisation with excellent employee retention.
- Why this job: Make a real impact in clinical research while working with a collaborative team.
- Qualifications: 3-5 years of medical writing experience and a strong background in the pharmaceutical industry.
The predicted salary is between 50000 - 65000 £ per year.
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognised for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
We are looking for a full-time employee, remotely based within the UK.
Responsibilities
- Under minimal supervision, the Medical Writer will critically evaluate, analyse, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
- Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals.
- Complete writing assignments in a timely manner.
- Maintain timelines and workflow of writing assignments.
- Practice good internal and external customer service.
- Highly proficient with styles of writing for various regulatory documents.
- Expert proficiency with client templates & style guides.
- Interact directly and independently with clients to coordinate all facets of projects; competent communicator skills for projects.
- Contribute substantially to, or manage, production of interpretive guides.
- Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary.
- Mentor medical writers and other members of the project team who are involved in the writing process.
Requirements
- At least 3 years of previous experience in the pharmaceutical industry.
- Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience.
- The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline.
- Substantial clinical study protocol experience, as lead author, required.
- Experience leading and managing teams while authoring regulatory documents with aggressive timelines.
- Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus.
- Understanding of clinical data.
- Exceptional writing skills are a must.
- Excellent organisational skills and the ability to multi-task are essential prerequisites.
- Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools.
- Experience being a project lead, or managing a project team.
- Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus.
- Not required, but experience with orphan drug designations and PSP/PIPs a plus.
Senior Medical Writer (Remote - UK) in Wales employer: MMS
At MMS, we are committed to fostering a supportive and innovative work culture that empowers our employees to make meaningful contributions in the field of clinical research. As a Great Place to Work certified organisation, we offer exceptional employee retention rates, opportunities for professional growth, and a collaborative environment that values diversity and inclusion. Join us remotely from the UK and be part of a team that is not only shaping the future of clinical research but also prioritising your career advancement and well-being.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Medical Writer (Remote - UK) in Wales
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant webinars, and join online forums. The more people you know, the better your chances of landing that Senior Medical Writer role at MMS.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical research and regulatory writing. Be ready to discuss your past experiences and how they align with MMS's mission. Show them you're not just a fit, but the perfect fit!
✨Tip Number 3
Don’t forget to showcase your writing skills! Bring samples of your previous work to the interview. This is your chance to demonstrate your expertise in crafting clinical documents and impress the hiring team at MMS.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, it shows your enthusiasm for joining a company that values innovation and collaboration like MMS.
We think you need these skills to ace Senior Medical Writer (Remote - UK) in Wales
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Medical Writer role. Highlight your relevant experience in regulatory writing and clinical documents, and don’t forget to showcase your exceptional writing skills!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your background makes you a perfect fit for our innovative team at MMS.
Showcase Your Experience:When detailing your experience, focus on specific projects where you’ve led or contributed significantly. Mention any regulatory submissions you’ve worked on, as this will resonate with us at MMS.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at MMS
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical writing and regulatory documents. Familiarise yourself with the specific types of documents mentioned in the job description, like clinical protocols and study reports. This will show that you're not just a good writer, but also understand the nuances of the industry.
✨Showcase Your Experience
Prepare to discuss your previous experience in the pharmaceutical industry, especially any leadership roles you've had. Be ready to share specific examples of projects you've led or contributed to, particularly those involving regulatory submissions. This will help demonstrate your capability and confidence.
✨Ask Insightful Questions
Interviews are a two-way street! Prepare some thoughtful questions about MMS's culture, team dynamics, and their approach to clinical research. This shows that you're genuinely interested in the company and want to ensure it's a good fit for you too.
✨Demonstrate Your Communication Skills
As a Medical Writer, clear communication is key. During the interview, focus on articulating your thoughts clearly and concisely. You might even want to practice explaining complex concepts in simple terms, as this will reflect your ability to communicate effectively with both clients and team members.
