Clinical Research Associate (CRA)

Placements24; George; Hybrid; ZAR 540,000 - 900,000; Full time

Benefits offered by this job

Hybrid work model

Company car or travel allowance

Professional development support

Job summary

Placements24 is seeking a dedicated Clinical Research Associate (CRA) to support ongoing clinical trials in the George region. You will monitor sites, verify protocol compliance, and maintain accurate trial documentation to ensure data integrity.

This hybrid role combines field visits with remote work, offering flexibility while ensuring on-site oversight. You will collaborate with investigators, site staff, and internal teams to advance pharmaceutical development in the Western Cape.

Qualifications

• Bachelor's degree in life sciences, nursing, or related field
• 4+ years of CRA experience
• Proficiency in ICH-GCP and regulatory requirements
• Experience with EDC and CTMS/clinical trial software
• Excellent organization and communication skills

Responsibilities

• Conduct site initiation, monitoring, and close-out visits
• Verify data accuracy in CRFs/EDC systems
• Communicate with sponsor and sites to resolve issues
• Ensure compliance with GCP and local/international regulations
• Prepare monitoring visit reports with findings and corrective actions

Skills

Site monitoring

Data verification

GCP/ICH compliance

Communication

Education

Bachelor's degree in life sciences

Tools

EDC systems

CTMS

Job description

About the Role Our client is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to support ongoing clinical trials in the George region. This role is crucial for ensuring the integrity and quality of trial data by monitoring clinical sites, verifying compliance with protocols, and maintaining accurate documentation. You will be instrumental in facilitating the smooth operation of clinical studies, working closely with investigators, site staff, and internal project teams to advance pharmaceutical development in Western Cape . This position offers a blend of field visits and remote work, providing flexibility while ensuring essential on-site oversight.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits to ensure adherence to study protocols and regulatory requirements.
• Verify the accuracy, completeness, and validity of clinical data recorded in case report forms (CRFs) and electronic data capture (EDC) systems.
• Manage communication between the sponsor and clinical trial sites, addressing queries and resolving issues promptly.
• Ensure compliance with Good Clinical Practice (GCP) guidelines and all applicable local and international regulations.
• Prepare and present monitoring visit reports, highlighting findings and recommending corrective actions.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 4 years of experience as a Clinical Research Associate, with a strong understanding of clinical trial processes.
• Proficiency in ICH-GCP guidelines and relevant regulatory requirements.
• Experience with EDC systems and clinical trial management software.
• Excellent organizational, communication, and interpersonal skills, with a keen eye for detail.

Benefits

• Competitive annual salary with performance incentives.
• Comprehensive medical, dental, and vision coverage.
• Company car or travel allowance for site visits.
• Support for professional development and continuous learning.
• A hybrid work model offering flexibility for employees in George and surrounding areas.