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Senior Scientific Document Reviewer (Home Based - South Africa)
Senior Scientific Document Reviewer (Home Based - South Africa)MMS Holdings Inc • WorkFromHome, Eastern Cape, South Africa
Senior Scientific Document Reviewer (Home Based - South Africa)

Senior Scientific Document Reviewer (Home Based - South Africa)

MMS Holdings Inc • WorkFromHome, Eastern Cape, South Africa
22 hours ago
Job type
  • Remote
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.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn.

Scientific Document Reviewer

This position is a fulltime home-based role out of any locationin South Africa.

Job Specific Skills :

  • Proficient with templates, toolbars, and macros
  • Able to adapt to differentclient styleguides and document formatting requirements
  • Proficient with correcting grammar & spelling errors, with ensuring intra- and inter-document consistency
  • Proficient withensuring scientificsenseand the correctness ofdata interpretation
  • Proficient withthe QC of a wide range of regulatory documents, including

Investigators Brochure

  • Protocols, protocol amendments and summaries of changes
  • ICFs and ICF amendments
  • CSRs (synoptic, abbreviated, interim, full, addendum)
  • Briefing Documents and Meeting Requests
  • Assessment Aids
  • Health Authority Responses
  • CTD clinical modules (especially strong experience with 2.7.1, 2.7.2, ISI)
  • Additionally, proficient withthe 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 fieldis preferred,butrelevant QCexperienceis acceptable
  • Minimum of 5 years’ experience in Quality Control or similar field required.
  • Proficiency with MSWord and Excel.
  • Clear and timelycommunication, ableto work with others to clearly understand needs and solve problems.
  • Basic understanding of CROs and scientific & clinical data / terminology, & the drug development process.
  • If you have not received a response within 14 days of your application, please consider your application unsuccessful.

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    Reviewer South Based • WorkFromHome, Eastern Cape, South Africa

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