Available Position (Company name withheld)

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.

Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.

MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.

Please note that this is a Project-based opportunity requiring up to 40 hours per week support until the end of July 2026

Roles and Responsibilities

• Proficient with Microsoft Word, including working with templates, toolbars, and macros
• Able to adapt to different author style guides and document formatting requirements
• Proficient with correcting grammar & spelling errors, with ensuring intra- and inter-document consistency
• Proficient with ensuring scientific sense and the correctness of data interpretation
• Proficient with checking in-text data with source tables
• Proficient with the QC of a wide range of regulatory documents, including
  • Investigators Brochure
  • Protocols, protocol amendments and summaries of changes
  • Informed consent documents
  • Clinical Study Reports (synoptic, abbreviated, interim, full, addendum)
  • Briefing Documents and Meeting Requests
  • Assessment Aids
  • Health Authority Responses
  • ICH Submission documents for clinical trial licencing (especially strong experience with 2.7.1, 2.7.2, 2.7.3, 2.7.4, ISE/S/I)
• Additionally, proficient with the QC of a wide range of med comms documents would be advantageous but not necessary, including
  • Slide Decks
  • Posters
  • Abstracts
  • Manuscripts

Job Requirements:

• College graduate in a scientific, medical, clinical discipline or related field is preferred, but relevant QC or Editorial experience is acceptable
• Minimum of 3 years’ experience in Quality Control or similar field required.
• Proficiency with MS Word and Excel.
• Clear and timely communication, able to work with others as part of a matrix organisation, to clearly understand and work to operational processes, to proactively solve problems without direction and to work as part of an international team.
• Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.