Senior Scientific Document Reviewer (Home Based - South Africa)

MMS Holdings Inc.; Remote; ZAR 400 000 - 600 000; Full time

Job summary

A leading clinical research organization in South Africa is seeking a Scientific Document Reviewer for a fulltime home-based role. Ideal candidates will have over 5 years of Quality Control experience, proficiency in MS Word and Excel, and a background in scientific, medical, or clinical disciplines. Responsibilities include ensuring the accuracy of various regulatory documents and adapting to client style guides. Join a supportive and innovative team committed to excellence in clinical research.

Qualifications

• Minimum of 5 years’ experience in Quality Control or similar field required.
• Clear and timely communication skills are essential.
• Basic understanding of CROs and scientific data/terminology is preferred.

Responsibilities

• Ensure accuracy and consistency of scientific documents.
• Perform quality control on regulatory submissions.
• Adapt documents to various client style guides.

Skills

Proficient with templates, toolbars, and macros

Able to adapt to different client style guides

Proficient with grammar & spelling corrections

Ensuring scientific correctness of data interpretation

QC of a wide range of regulatory documents

Education

College graduate in a scientific, medical, or clinical discipline

Tools

MS Word

Excel

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.

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, 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 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 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.