Clinical Research Associate (CRA)

Placements24; Johannesburg; On-site; ZAR 450,000 - 750,000; Full time

Job summary

Placements24 represents a renowned pharmaceutical company seeking a diligent Clinical Research Associate to join the team in Rustenburg, North West. This field-based role requires extensive travel to clinical trial sites and focuses on monitoring trial conduct, data integrity, and patient safety.

The ideal candidate holds a Life Sciences degree with at least 3 years of CRA experience and a working knowledge of GCP/ICH guidelines, CTMS, and EDC systems.

Qualifications

• Bachelor’s degree in Life Sciences or related field is required.
• Minimum 3 years of experience as a CRA.
• Knowledge of GCP/ICH guidelines and regulatory requirements.
• Experience with CTMS and EDC systems.
• Willingness to travel up to 70%.

Responsibilities

• Conduct site initiation, monitoring, and close-out visits.
• Ensure data accuracy and integrity across trials.
• Verify source data against CRFs.
• Maintain study documentation at investigator sites.
• Build relationships with investigators and site staff.
• Monitor patient safety and report adverse events.
• Ensure compliance with GCP, FDA regulations, and guidelines.
• Provide training to site personnel.

Skills

Organizational skills

Time management

Problem-solving

Written and verbal communication

Education

Bachelor's degree in Life Sciences

Tools

CTMS

EDC systems

Job description

About the Role

Our client, a renowned pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team in Rustenburg, North West . This is a field-based role requiring extensive travel to clinical trial sites. As a CRA, you will be responsible for monitoring clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulations. You will play a vital role in the successful execution of clinical studies, contributing directly to the development of new medicines. This position demands a highly organized individual with strong attention to detail and excellent interpersonal skills.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits for clinical trials.
• Ensure the accuracy, completeness, and integrity of clinical trial data.
• Verify source data against case report forms (CRFs).
• Manage and maintain study documentation at investigator sites.
• Build and maintain strong relationships with investigators, site staff, and study participants.
• Monitor patient safety and report adverse events as per protocol and regulatory requirements.
• Ensure compliance with GCP, FDA regulations, and other relevant guidelines.
• Troubleshoot and resolve site-level issues to ensure trial progress.
• Provide training to site personnel on study protocols and procedures.

Requirements

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate.
• Comprehensive knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven ability to conduct site monitoring visits and manage study sites effectively.
• Excellent organizational, time management, and problem-solving skills.
• Strong written and verbal communication skills, with the ability to present information clearly.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel extensively (up to 70%) within the assigned region.
• Valid driver's license and reliable transportation.

Benefits

Our client offers a competitive salary, a travel allowance, and a comprehensive benefits package including medical aid and a retirement fund. Opportunities for professional growth and career advancement within a leading pharmaceutical organization are readily available. You will be part of a dedicated team contributing to life-saving medical advancements. This role provides the opportunity to work closely with healthcare professionals and make a significant impact on clinical research in the Rustenburg area.