Clinical Research Associate (CRA) - Pharmaceutical

Placements24; Pretoria; On-site; ZAR 720,000 - 940,000; Full time

Benefits offered by this job

Salary with performance-based bonuses

Medical insurance

Company car / travel allowance

Hybrid work arrangement

Job summary

Placements24 is seeking a skilled Clinical Research Associate to support pharmaceutical trials based in Pretoria. You will monitor trial sites, ensure protocol compliance, and collect accurate data to support drug development.

The role requires extensive travel within Gauteng and beyond, with a hybrid work arrangement balancing field visits and remote tasks. Key requirements include a bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field, at least 3 years as a CRA, strong GCP

Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
• 3+ years as a Clinical Research Associate in pharma.
• Strong knowledge of GCP and regulatory requirements.

Responsibilities

• Conduct site initiation, monitoring and close-out visits per protocol and GCP.
• Ensure rights, safety and well-being of trial participants.
• Verify accuracy and integrity of data collected at study sites.
• Maintain clear communication with investigators and site staff.
• Oversee site adherence to protocol, SOPs and regulatory requirements.
• Manage essential trial documents and site regulatory binders.

Skills

GCP knowledge

Monitoring skills

Data verification

Communication

Travel readiness

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field

Tools

CTMS

EDC systems

Job description

Our client is seeking a skilled Clinical Research Associate (CRA) to support their pharmaceutical clinical trials based in Pretoria . You will be responsible for monitoring clinical trial sites, ensuring compliance with protocols, and collecting accurate data to support drug development. This role requires extensive travel to investigational sites within Gauteng and potentially beyond. It's a vital position within the drug development lifecycle, offering a chance to make a significant impact on bringing new medicines to patients.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits according to the clinical trial protocol and GCP guidelines.
• Ensure the rights, safety, and well-being of trial participants are protected.
• Verify the accuracy, completeness, and integrity of clinical data collected at study sites.
• Maintain effective communication with investigators, site staff, and the internal study team.
• Oversee site adherence to the study protocol, SOPs, and applicable regulatory requirements.
• Manage essential trial documents and site regulatory binders.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Excellent monitoring skills, including source data verification and query resolution.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness and ability to travel extensively within Pretoria and surrounding areas for site visits.

Benefits

• Competitive annual salary with performance-based incentives.
• Comprehensive medical, dental, and vision insurance plans.
• Company car or travel allowance for site visits.
• Opportunities for professional growth and advanced training in clinical research.
• A hybrid working arrangement that combines fieldwork with remote administrative tasks.