Senior Medical Writer (Remote - UK)

MMS; Swansea; On-site; GBP 42,000 - 65,000; Full time

Job summary

MMS is a data-focused clinical research organization recruiting a Medical Writer for a remote UK role. You will craft regulatory documents, lead author regulatory sections, and coordinate with cross-functional teams to ensure project success.

The ideal candidate has 3–5 years in pharma writing, strong MS Word skills, and experience with regulatory submissions, while enjoying a supportive, innovative team culture at MMS.

Qualifications

• At least 3 years of experience in the pharmaceutical industry.
• 3-5 years of industry regulatory writing and clinical medical writing experience.
• Ideal candidate would hold a Bachelor’s, Master’s or PhD in scientific/medical 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.
• Excellent organizational skills and ability to multi-task.

Responsibilities

• Under minimal supervision, critically evaluate, analyze, and interpret medical literature for study design and regulatory rigor.
• Write and edit clinical development documents including protocols, investigator's brochures, study reports, consent forms, and modules.
• Complete writing assignments in a timely manner and maintain timelines/workflows.
• Interact directly with clients to coordinate project aspects and mentor medical writers.

Skills

Regulatory writing

Medical writing

Client communication

Project leadership

Regulatory submissions

Education

Bachelor's/Master's/PhD in scientific or medical field

Tools

MS Word

Excel

PowerPoint

Job description

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 a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized 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, analyze, 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 client to coordinate all facets of projects; competent communicator skills for projects
• Contribute substantially to, or manages, 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 organizational 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
• Substantial clinical study protocol experience, as lead author, required
• Experience leading and managing teams while authoring regulatory documents with aggressive timelines
• Not required, but experience with orphan drug designations and PSP/PIPs a plus