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. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn. Associate Medical Writer We are recruiting for an Associate Medical Writer to join our UK team. This position is a home-based role out of any location in the UK. Job Specific Skills Has basic understanding of regulations and guidance as they pertain to medical writing. Trained on styles of writing for various document types. Has understanding of QC process. Trained on general instructions on process, detailed instructions on MW deliverables and client/MMS processes. Trained on templates, toolbars and formatting. Understands MMS and client processes and training; is 100% compliant. Has basic understanding of impact of updates in related deliverables. Trained on managing client meetings and CRMs. Trained and has basic understanding of managing a project from start to finish. Has basic understanding of identifying and mitigating project risk, including assessing client gaps. Has basic understanding of handling client feedback Can set up QC trackers. Can lead projects with guidance. Can incorporate straightforward comments. Can format documents. Job Requirements College graduate in scientific, medical, clinical discipline or related field, or related experience, masters or PhD preferred. 0-2 years of experience in Medical Writing or similar field preferred/required. Knowledge of scientific principles and concepts. Proficiency with MS Office applications. Hands-on experience with clinical trial and pharmaceutical development preferred. Good communication skills and willingness to work with others to clearly understand needs and solve problems. Excellent problem-solving skills. Good organizational and communication skills. Familiarity with current ISO 9001 and ISO 27001 standards preferred. Familiarity with 21 CFR Part 11, FDA, and GCP requirements. Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process. Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.