Clinical Research Associate

Placements24; Rustenburg; Hybrid; ZAR 520,000 - 760,000; Full time

Benefits offered by this job

Competitive salary

Medical, dental, vision benefits

Company car or travel allowance

Retirement fund contribution

Professional development opportunities

Flexible working arrangements

Job summary

Placements24 seeks a diligent Clinical Research Associate to support clinical trials in the Rustenburg area with a hybrid work setup. You will monitor sites, review data, and ensure adherence to protocols, SOPs, and regulatory requirements, while coordinating with investigators and study teams.

The role requires a Life Sciences degree, at least 3 years of CRA experience, and strong GCP knowledge. Travel to sites and remote-task management are expected in this position.

Qualifications

• Bachelor's degree in Life Sciences or related field is required.
• Minimum 3 years of CRA or similar experience in clinical trials.
• Strong understanding of GCP and regulatory guidelines.

Responsibilities

• Monitor clinical trial sites for protocol compliance and data integrity.
• Review source data and case report forms for accuracy and completeness.
• Communicate trial progress and issues with investigators and teams.
• Identify and resolve deviations or potential issues in trials.
• Ensure timely recruitment and adherence to timelines.
• Conduct site initiation, monitoring, and close-out visits as needed.

Skills

GCP knowledge

Site monitoring

Regulatory compliance

Data management

Communication

Time management

Education

Bachelor's degree in Life Sciences

Tools

CTMS

eCRF systems

Clinical trial software

Job description

About the Role

Our client is seeking a diligent and detail-oriented Clinical Research Associate to contribute to the successful execution of clinical trials. This hybrid role balances remote work flexibility with essential on-site responsibilities for patient interaction and site management within the Rustenburg area. You will be integral in ensuring that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, and regulatory requirements. Your work will directly impact the integrity and validity of our research data, supporting the development of life-changing therapies. This position requires a proactive approach and the ability to manage your workload efficiently across both remote and field-based tasks.

Key Responsibilities

• Monitor clinical trial sites to ensure compliance with protocols, regulations, and data integrity.
• Manage and review clinical trial documentation, including source data and case report forms.
• Communicate effectively with investigators, site staff, and internal study teams regarding trial progress and issues.
• Identify, assess, and resolve potential issues or deviations encountered during clinical trials.
• Ensure timely recruitment of participants and adherence to study timelines.
• Conduct site initiation, monitoring, and close-out visits as required.

Requirements

• Bachelor's degree in Life Sciences, Nursing, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate or similar role.
• Strong understanding of Good Clinical Practice (GCP) and relevant regulatory guidelines.
• Proficiency in clinical trial management software and electronic data capture systems.
• Excellent organizational, time management, and problem-solving skills.
• Ability to travel to clinical sites as needed and effectively manage remote work tasks.

Benefits

• Competitive annual salary with performance-based incentives.
• Comprehensive medical, dental, and vision benefits package.
• Company car or travel allowance for site visits.
• Retirement fund contribution.
• Opportunities for professional development and certifications.
• Flexible working arrangements with a balance of remote and in-office duties.