Remote Clinical Data Associate II — Global Trials

Ali Aydi; South Africa; À distance; ZAR 600 000 - 720 000; Plein temps

Avantages offerts par ce poste

Medical Aid Contribution

Gap Cover

Life Assurance

13th Cheque

Résumé du poste

Parexel is seeking a Clinical Data Associate II to join our South Africa team in a remote capacity. You will support global clinical research programs by delivering high-quality data management activities across Phase I-IV studies, ensuring data quality and regulatory compliance.

You will collaborate with clinical teams, statisticians, programmers, CRAs, vendors, and study management to manage data capture, queries, reconciliation, and database activities, contributing to study deliverables and

Qualifications

• Bachelor’s degree in a scientific or healthcare field.
• Minimum two years’ experience in Data Management in pharma/biotech.
• Solid knowledge of ICH/FDA, CDISC, GCDMP, 21 CFR Part 11, MedDRA, and WHO Drug dictionaries.
• Experience with EDC systems; RAVE preferred.

Responsabilités

• Lead/co-lead data management activities for Phase I–IV studies.
• Coordinate EDC systems design, testing, and issue resolution.
• Review study protocols and develop annotated eCRFs.
• Develop data management plans and SOPs; support data quality inspections.
• Manage data queries, external data reconciliations, and SAE reconciliation.

Connaissances

Attention to detail

Analytical thinking

Organizational skills

Clinical data management

Formation

Bachelor's Degree in science/healthcare

Outils

RAVE

eCRF design

Description du poste

Parexel is seeking a Clinical Data Associate II to join our South Africa team in a remote capacity. You will support global clinical research programs by delivering high-quality data management activities across Phase I-IV studies, ensuring data quality and regulatory compliance.

You will collaborate with clinical teams, statisticians, programmers, CRAs, vendors, and study management to manage data capture, queries, reconciliation, and database activities, contributing to study deliverables and