Clinical Data Manager: Data Integrity & EDC Lead

Placements24; Klerksdorp; Hybrid; ZAR 600,000 - 1,000,000; Full time

Benefits offered by this job

Competitive salary

Bonus incentives

Medical and dental insurance

Retirement savings plan

Generous annual leave

Training and development

Collaborative research environment

Impactful medicines

Job summary

Placements24 is seeking a detail-oriented Clinical Data Manager to join our pharmaceutical client in Soweto, Gauteng. You will oversee database design, data validation, query management, and data reconciliation to ensure data integrity for regulatory submissions.

The role requires hands-on experience with EDC systems (Medidata Rave, Oracle Clinical, Veeva EDC), strong knowledge of GCP, and the ability to collaborate with clinical teams, biostatisticians, and IT staff.

Qualifications

• Bachelor’s degree in a scientific, technical, or healthcare-related field.
• 3–5 years of experience in clinical data management in pharma/biotech/CRO.
• Proficiency with EDC systems (Medidata Rave, Oracle Clinical, Veeva EDC).
• Strong understanding of GCP, ICH guidelines, and regulatory processes.

Responsibilities

• Oversee design, development, and maintenance of clinical databases using EDC systems.
• Develop and execute data management plans and validation plans.
• Define data validation specs and implement edit checks for data quality.
• Manage data cleaning, queries with investigative sites, and data reconciliation.
• Coordinate database lock activities with study teams.
• Ensure compliance with regulatory requirements and SOPs.
• Maintain study-specific data management documentation and updates.

Skills

Data management

Regulatory awareness

Analytical skills

Communication

Teamwork

Problem-solving

Education

Bachelor's degree in a scientific/technical/healthcare field

Tools

Medidata Rave

Oracle Clinial

Veeva EDC

Job description

Placements24 is seeking a detail-oriented Clinical Data Manager to join our pharmaceutical client in Soweto, Gauteng. You will oversee database design, data validation, query management, and data reconciliation to ensure data integrity for regulatory submissions.

The role requires hands-on experience with EDC systems (Medidata Rave, Oracle Clinical, Veeva EDC), strong knowledge of GCP, and the ability to collaborate with clinical teams, biostatisticians, and IT staff.