Clinical Research Associate (CRA) - Oncology

Placements24; Rustenburg; On-site; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Company car/allowance

Health insurance

Paid time off

Travel allowance

Training & development

Job summary

Placements24 is seeking an experienced Oncology-focused Clinical Research Associate (CRA) to join our field-based operations in Rustenburg, North West. You will monitor trial sites, ensure GCP compliance, and collaborate with sponsors to drive patient safety and data integrity.

The role requires up to 70% travel, strong communication, and hands-on monitoring across sites, with opportunities for professional growth within a reputed pharmaceutical setting.

Qualifications

• Bachelor’s degree in life sciences, nursing or related field.
• Minimum 3 years as a Clinical Research Associate with oncology focus.
• Solid understanding of ICH-GCP and regulatory requirements.
• Experience in site monitoring visits and data verification.
• Excellent interpersonal and communication skills for site liaison.
• Ability to travel extensively within the region (up to 70%).
• Proficiency with EDC systems and CTMS.

Responsibilities

• Conduct pre-study, initiation, interim and close-out visits at trial sites.
• Monitor study conduct for protocol, GCP, and regulatory compliance.
• Verify data accuracy in source documents and CRFs.
• Manage site issues with CAPAs as needed.
• Ensure timely enrollment and protocol adherence.
• Maintain communication with investigators and internal teams.
• Oversee drug accountability and site supplies.
• Prepare trial status updates and site performance metrics.
• Maintain regulatory documentation at sites.
• Assist in site selection and feasibility for new trials.

Skills

Oncology CRA experience

GCP regulatory knowledge

Site monitoring & data verification

Strong communication & interpersonal

Travel up to 70%

EDC/CTMS proficiency

Education

Bachelor's degree in life sciences/nursing or related field

Tools

EDC systems

CTMS

Job description

About the Role

Our client is actively seeking a dedicated and experienced Clinical Research Associate (CRA) specializing in Oncology to join their growing clinical operations team based in Rustenburg, North West . This is a field-based position crucial for overseeing and managing the progress of clinical trials at investigative sites. You will be instrumental in ensuring the quality, integrity, and compliance of clinical research activities, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. This role demands a high level of autonomy, strong interpersonal skills, and a proactive approach to problem-solving within the demanding landscape of cancer research. You will act as the primary liaison between the study sponsor and the clinical sites, fostering strong relationships and facilitating efficient trial execution. Your commitment to accuracy and patient safety will be paramount as you contribute to the development of novel cancer therapies. This is an excellent opportunity for a seasoned CRA looking to make a significant contribution to advancing oncology treatments within a reputable pharmaceutical organization committed to excellence in clinical research execution.

Key Responsibilities

• Conduct pre-study, initiation, interim, and close-out visits at clinical trial sites.
• Monitor study conduct to ensure adherence to the protocol, GCP, and applicable regulations.
• Verify the accuracy, completeness, and integrity of clinical data recorded in source documents and case report forms (CRFs).
• Manage site issues, implementing corrective and preventive actions as needed.
• Ensure timely enrollment of subjects and facilitate protocol adherence.
• Maintain effective communication with investigators, site staff, and internal study teams.
• Oversee drug accountability and manage study supplies at the site level.
• Prepare and present trial status updates and site performance metrics.
• Ensure all required regulatory documentation is maintained at the investigative sites.
• Contribute to site selection and feasibility assessments for new clinical trials.

Requirements

• Bachelor's degree in a life science, nursing, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
• Thorough understanding of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
• Proven experience in conducting site monitoring visits and data verification.
• Excellent interpersonal and communication skills, with the ability to build rapport with site personnel.
• Strong organizational and time management abilities, with the capacity to manage multiple priorities effectively.
• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Ability to travel extensively within the assigned region (up to 70% travel required).
• Detail-oriented with a commitment to data accuracy and patient safety.
• Valid driver's license and a reliable vehicle.

Benefits

• Highly competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous travel allowance and expense reimbursement.
• Company car or car allowance provided.
• Retirement savings plan with employer contributions.
• Paid time off and public holidays.
• Continuous training and professional development opportunities.
• Access to innovative clinical trial technologies.
• Supportive team environment and experienced management.
• The chance to work on groundbreaking cancer treatments.