Senior Scientific Document Reviewer (Home Based - South Africa)

MMS Holdings Inc.; Remote; ZAR 200 000 - 300 000; Full time

Job summary

A leading clinical research organization in South Africa is seeking a Scientific Document Reviewer for a full-time home-based role. The position requires a minimum of 5 years of Quality Control experience, proficiency in MS Word and Excel, and an understanding of scientific data and the drug development process. You will be responsible for ensuring document consistency and compliance with various standards. If you're looking to contribute to a collaborative team that shapes clinical research, this opportunity is for you.

Qualifications

• Minimum of 5 years’ experience in Quality Control or similar field.
• Clear and timely communication skills.
• Basic understanding of CROs and drug development process.

Responsibilities

• Ensure consistency in documents and adhere to client style guides.
• Conduct quality control of a wide range of regulatory documents.
• Adapt to document formatting requirements.

Skills

Proficient with templates, toolbars, and macros

Adapt to different client style guides

Correcting grammar & spelling errors

Ensuring scientific sense and data interpretation

Quality control of regulatory documents

Proficient with MS Word

Proficient with MS Excel

Education

College graduate in a scientific, medical, or clinical discipline

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 .

Scientific Document Reviewer

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

Job Specific Skills

• Proficient with templates, toolbars, and macros
• Able to adapt to different client 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 the QC of a wide range of regulatory documents, includingInvestigators BrochureProtocols, protocol amendments and summaries of changesICFs and ICF amendmentsCSRs (synoptic, abbreviated, interim, full, addendum)Briefing Documents and Meeting RequestsAssessment AidsHealth Authority ResponsesCTD clinical modules (especially strong experience with 2.7.1, 2.7.2, ISI)
• Additionally, proficient with the QC of a wide range of med comms documents would be advantageous but not necessary, includingSlide DecksPostersAbstractsManuscripts

Job Requirements

• College graduate in a scientific, medical, clinical discipline or related field is preferred, but relevant QC experience is acceptable
• Minimum of 5 years’ experience in Quality Control or similar field required.
• Proficiency with MS Word and Excel.
• Clear and timely communication, able to 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.