Senior RAVE Clinical Data Architect for Trials

MMS Holdings Inc; Johannesburg; On-site; ZAR 900,000 - 1,200,000; Full time

Job summary

MMS Holdings Inc is seeking a Senior Clinical Database Developer (Rave) to join a data-focused CRO. You will contribute to protocol reviews, data capture, and CRF tracking, while ensuring data integrity across multiple EDC systems.

The role requires 5+ years in clinical database programming, strong Rave build skills, and expert custom function programming. You will work with cross-functional teams to deliver timely, compliant study data and support UAT and training.

Qualifications

• Minimum 5 years of clinical database programming experience.
• Strong Rave Study Build skills.
• Expert Custom Function programming is mandatory.
• College graduate in computer science or related discipline.
• Experience in drug development and clinical trials.

Responsibilities

• Participates in protocol review with clients and helps capture data in the database.
• Contributes to study tracking and metric reports for the study team.
• Contributes to CRF tracking, data entry, external data integration, validation and QC.
• Performs UAT of EDC and integrated systems, including test plans and scripts.
• Trains sites/users on EDC applications and UAT.
• Maintains end-user knowledge for study conduct and query management.
• Develops data listing and edit checks as appropriate.
• Assists with study documentation and database design.

Skills

Clinical DB programming

Rave Study Build

Custom Function programming

Data management

Pharma/CRO knowledge

Education

College degree in computer science or related discipline

Tools

SQL

SAS

Rave

Job description

MMS Holdings Inc is seeking a Senior Clinical Database Developer (Rave) to join a data-focused CRO. You will contribute to protocol reviews, data capture, and CRF tracking, while ensuring data integrity across multiple EDC systems.

The role requires 5+ years in clinical database programming, strong Rave build skills, and expert custom function programming. You will work with cross-functional teams to deliver timely, compliant study data and support UAT and training.