Clinical Research Associate (CRA) - Oncology

Placements24; Centurion; Hybrid; ZAR 550,000 - 900,000; Full time

Benefits offered by this job

Medical aid

Provident fund

Life insurance

Job summary

Placements24 seeks an experienced Clinical Research Associate (Oncology) to monitor study sites, verify patient records, and ensure strict adherence to protocols and regulatory standards. The role blends on-site monitoring with remote reporting and administration from Centurion, South Africa.

The ideal candidate has 3–5 years in oncology-focused CRA roles, strong GCP knowledge, and excellent communication skills to collaborate with investigators and site staff.

Qualifications

• Bachelor’s degree in a life science, nursing, or related field.
• 3–5 years of CRA experience with a focus on oncology trials.
• Strong understanding of GCP and regulatory requirements (ICH, FDA, EMA, SAHPRA).
• Experience in site monitoring, data review, and query resolution.

Responsibilities

• Conduct site initiation, routine monitoring, and close-out visits per protocols and GCP.
• Verify data accuracy by reviewing source documents and CRFs.
• Manage data queries and maintain data integrity.
• Assess site staff adherence to protocols and consent procedures.
• Serve as primary contact for assigned sites and build investigator relationships.
• Ensure investigational product management and drug dispensing at sites.
• Identify risks at sites and implement mitigation strategies.
• Prepare monitoring reports and follow-up on actions.
• Maintain knowledge of oncology treatments and trial regulations.

Skills

Oncology trials

Site monitoring

GCP compliance

Data query resolution

Excellent communication

Travel up to 50%

Education

Bachelor's degree in life science or nursing

Tools

EDC systems

Clinical trial management software

Job description

About the Role

Our client, a globally recognized contract research organization (CRO) focused on delivering innovative clinical trial solutions, is seeking a diligent and experienced Clinical Research Associate (CRA) specializing in Oncology to join their team in Centurion, Gauteng, ZA. This role is crucial for ensuring the integrity and accuracy of clinical trial data by monitoring study sites, verifying patient records, and ensuring adherence to protocols and regulatory requirements. The successful candidate will be instrumental in advancing critical cancer research. This is a hybrid position, blending essential on-site monitoring activities with the flexibility of remote work for reporting and administrative tasks. The role requires a highly organized individual with a keen eye for detail and a passion for contributing to life-changing medical advancements.

Key Responsibilities

• Conduct site initiation visits, routine monitoring visits, and close-out visits to ensure compliance with study protocols, GCP, and regulatory guidelines.
• Verify accuracy and completeness of clinical data by reviewing source documents, case report forms (CRFs), and electronic data capture (EDC) systems.
• Manage and resolve data queries in a timely manner, ensuring data integrity.
• Assess site staff adherence to protocol requirements, informed consent procedures, and regulatory standards.
• Serve as the primary point of contact for assigned clinical trial sites, building strong relationships with investigators and site staff.
• Ensure proper investigational product management, accountability, and drug dispensing at study sites.
• Identify potential risks and issues at clinical sites and implement appropriate mitigation strategies.
• Prepare detailed monitoring visit reports and follow-up on action items.
• Maintain up-to-date knowledge of oncology treatments, clinical trial methodologies, and relevant regulations.

Requirements

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3-5 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
• Strong understanding of Good Clinical Practice (GCP) guidelines and applicable regulatory requirements (e.g., ICH, FDA, EMA, SAHPRA).
• Proven experience in site monitoring, data review, and query resolution.
• Excellent organizational, time management, and communication skills.
• Ability to travel to clinical sites as required (up to 50%).
• Proficiency in EDC systems and clinical trial management software.
• Strong problem-solving abilities and attention to detail.Experience in therapeutic areas beyond oncology is a plus.
• Comfortable working in a hybrid model, balancing remote tasks with on-site responsibilities.

Benefits

Our client offers a competitive compensation package, including a generous salary, performance-based incentives, and a comprehensive benefits program covering medical aid, provident fund, and life insurance. Professional development opportunities include ongoing training, certifications, and exposure to diverse oncology research projects. This hybrid role in Centurion, Gauteng, ZA, provides a flexible working arrangement while ensuring you are at the forefront of groundbreaking cancer research. Enjoy a supportive team environment and the chance to make a tangible difference in patients' lives.