Senior Quality Control Reviewer - South Africa (Project-Based, Remote)

MMS Holdings Inc.; Durban; Remote; ZAR 500 000 - 700 000; Full time

Job summary

A leading clinical research organization in South Africa is seeking a Senior Quality Control Reviewer. The role requires at least 5 years of experience in Quality Control and proficiency in QC of various regulatory documents. Ideal candidates should be adept at ensuring data interpretation correctness and adapting to client style guides. The position offers a project-based opportunity of up to 40 hours per week, fostering a collaborative work environment.

Qualifications

• Minimum of 5 years’ experience in Quality Control or similar field required.
• Basic understanding of CROs and scientific & clinical data.
• Experience with QC of med comms documents is advantageous.

Responsibilities

• Proficient with the QC of a wide range of regulatory documents.
• Able to ensure scientific sense and correctness in data interpretation.
• Adapts to different client style guides and document formatting.

Skills

Proficient with templates, toolbars, and macros

Able to adapt to different client style guides

Correcting grammar & spelling errors

Ensuring intra- and inter-document consistency

Scientific sense and data interpretation correctness

QC of regulatory documents

Proficient with MSWord and Excel

Clear and timely communication

Education

College graduate in 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 an 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 .

This is a project‑based opportunity up to 40 hours per week.

Senior Quality Control Reviewer

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 MSWord 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.

Should you not have received a response within 14 days of your application, please consider your application unsuccessful.