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

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

Job summary

A leading clinical research organization is seeking a Senior Quality Control Reviewer for a project-based opportunity in Cape Town. This remote role requires a minimum of 5 years of experience in Quality Control, with proficiency in MS Word and Excel. The Reviewer will ensure the quality and scientific integrity of various regulatory documents. Strong communication abilities and a basic understanding of the drug development process are essential. Join a supportive and innovative team shaping clinical research's future.

Qualifications

• Minimum of 5 years’ experience in Quality Control or similar field required.
• Basic understanding of CROs and scientific & clinical data.
• Strong experience with regulatory documents.

Responsibilities

• Perform Quality Control on a range of regulatory documents.
• Ensure correctness of data interpretation and document consistency.
• Communicate clearly with team members to understand needs.

Skills

Proficient with templates, toolbars, and macros

Able to adapt to different client style guides

Proficient with correcting grammar & spelling errors

Proficient with ensuring scientific sense

Proficient with the QC of regulatory documents

Clear and timely communication

Proficiency with MS Word and Excel

Education

College graduate in a scientific, medical, clinical discipline

Job description

Senior Quality Control Reviewer - South Africa (Project-Based, Remote) MMS Holdings Inc.•Cape Town

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 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, 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.

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