Hybrid Clinical Research Associate: Trials & Data Integrity

Placements24; Bloemfontein; Hybrid; ZAR 420,000 - 560,000; Full time

Benefits offered by this job

Travel allowance

Medical insurance

Retirement fund

Professional development

Ethical environment

Job summary

Placements24 is seeking a dedicated Clinical Research Associate to support pharmaceutical clinical trials in the Welkom area. This hybrid role combines field-based activities with office responsibilities, focusing on site management, data integrity, and participant safety throughout the trial duration.

You will monitor sites per protocol and GCP, verify data via SDV, manage regulatory documents, and liaise between sites, the sponsor, and regulators.

Qualifications

• Bachelor's degree in a life science, nursing, or related field.
• Proven experience as a Clinical Research Associate or similar role.
• Strong knowledge of ICH-GCP guidelines and regulatory affairs.
• Experience with EDC and CTMS systems.
• Excellent communication and organizational skills.

Responsibilities

• Conduct site initiation, interim monitoring, and close-out visits per protocol and GCP.
• Verify data integrity through source data verification (SDV).
• Manage trial documentation including regulatory binders and accountability.
• Serve as main contact between sites, sponsor, and regulators.
• Identify and report adverse events per protocol.
• Train site staff on study procedures and data collection.

Skills

Organizational skills

Communication skills

Attention to detail

Multitasking

Problem solving

Team collaboration

Education

Bachelor’s degree in Life Science/Nursing or related field

Tools

EDC systems

CTMS

Job description

Placements24 is seeking a dedicated Clinical Research Associate to support pharmaceutical clinical trials in the Welkom area. This hybrid role combines field-based activities with office responsibilities, focusing on site management, data integrity, and participant safety throughout the trial duration.

You will monitor sites per protocol and GCP, verify data via SDV, manage regulatory documents, and liaise between sites, the sponsor, and regulators.