Quality jobs in South Africa
Senior Quality Control Reviewer - South Africa (Project-Based, Remote)
MMS Holdings Inc.
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Senior Quality Control Reviewer - South Africa (Project-Based, Remote)
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
Education
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.
- 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
- 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.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.