Clinical Research Associate (CRA) - Pharma

Placements24; Pretoria; Hybrid; ZAR 480,000 - 720,000; Full time

Benefits offered by this job

Competitive salary

Job summary

Placements24 is seeking a diligent Clinical Research Associate to oversee clinical trial conduct in the Pretoria region. You will monitor sites, ensure protocol adherence, and uphold GCP and regulatory standards while maintaining data integrity throughout studies.

The ideal candidate has a life sciences degree and at least three years of CRA experience, with strong communication skills and willingness to travel within the Pretoria area.

Qualifications

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of experience as a CRA in the pharmaceutical industry.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in site monitoring, data review, and query resolution.
• Ability to travel to clinical sites within the Pretoria area as needed.

Responsibilities

• Conduct site initiation, monitoring, and close-out visits according to study protocol and GCP requirements.
• Verify the accuracy, completeness, and timeliness of clinical data reported by study sites.
• Ensure regulatory compliance at clinical sites, including informed consent process and source data verification.
• Manage communication between study sites, the sponsor, and other stakeholders involved in the clinical trial.
• Identify, track, and resolve site-level issues and deviations promptly.
• Maintain accurate and organized study documentation and site files.

Skills

Clinical Research

GCP knowledge

Site monitoring

Data review

Query resolution

Communication

Education

Bachelors in life sciences

Job description

About the Role

Our client is seeking a diligent and proactive Clinical Research Associate (CRA) to oversee clinical trial conduct and ensure data integrity for pharmaceutical studies in the Pretoria region. As a key member of the clinical operations team, you will be responsible for monitoring clinical sites, ensuring adherence to study protocols, GCP guidelines, and all applicable regulations. This role demands exceptional organizational skills, meticulous attention to detail, and the ability to build strong relationships with investigators and site staff, contributing to the successful execution of critical clinical research projects that impact patient care.

Key Responsibilities

• Conduct site initiation, monitoring, and close-out visits according to study protocol and GCP requirements.
• Verify the accuracy, completeness, and timeliness of clinical data reported by study sites.
• Ensure regulatory compliance at clinical sites, including informed consent process and source data verification.
• Manage communication between study sites, the sponsor, and other stakeholders involved in the clinical trial.
• Identify, track, and resolve site-level issues and deviations promptly.
• Maintain accurate and organized study documentation and site files.

Requirements

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in site monitoring, data review, and query resolution.
• Excellent communication, organizational, and time management skills.
• Ability to travel to clinical sites within the Pretoria area as needed.

Benefits

• Competitive annual salary based on experience.
• Comprehensive medical and retirement benefits.
• Mileage and expense reimbursement for site visits.
• Opportunities for professional development and career advancement in clinical research.
• A dynamic and supportive work environment focused on bringing life-saving therapies to patients.