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Senior Quality Control Reviewer - South Africa (Project-Based, Remote)
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Senior Quality Control Reviewer - South Africa (Project-Based, Remote)
Job summary
A leading clinical research organization is seeking a Senior Quality Control Reviewer to ensure the accuracy of regulatory documents and data interpretation. The role requires a college degree in a relevant scientific field with at least 5 years of QC experience, plus proficiency in MS Word and Excel. This project-based opportunity involves collaboration and clear communication. Join us in shaping the future of clinical research in a supportive work environment.
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 & clinical data.
Responsibilities
- Proficient with QC of a wide range of regulatory documents.
- Ensure correctness of data interpretation.
- Work collaboratively to meet client needs.
Skills
Education
Tools
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. 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, 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 medical communications 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
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* 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.