Clinical Research Coordinator

Placements24; Bloemfontein; Hybrid; ZAR 300,000 - 420,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Paid time off

Professional development opportunities

Hybrid work schedule

Job summary

Placements24 is seeking a Clinical Research Coordinator in Welkom to support clinical trials with a balanced mix of on-site patient interactions and data management. The role emphasizes adherence to study protocols, regulatory standards, and data integrity, with attention to patient safety and collaboration across sponsors and investigators.

The ideal candidate has a Bachelor’s degree in a healthcare or scientific field, proven clinical research experience, and strong communication skills to

Qualifications

• Bachelor's degree in a healthcare or scientific field.
• Proven experience in clinical research.
• Strong understanding of GCP and regulatory requirements.
• Excellent organizational, time management, and multitasking abilities.
• Proficiency in electronic data capture (EDC) systems and medical terminology.
• Exceptional interpersonal and communication skills across diverse groups.

Responsibilities

• Coordinate day-to-day operations of clinical trials in line with study protocols and regulatory guidelines (ICH-GCP).
• Recruit, screen, and enroll eligible participants for clinical studies.
• Collect, process, and manage clinical data with accuracy, including source document verification.
• Schedule participant visits, tests, and procedures with meticulous record-keeping.
• Serve as liaison between investigators, participants, sponsors and regulators.
• Monitor patient safety and report adverse events per protocol requirements.

Skills

Excellent communication

Organizational skills

Time management

Multitasking

Empathy

Education

Bachelor's degree in healthcare or related field

Tools

EDC systems

Source document verification tools

Job description

About the Role

Our client is seeking a highly organized and motivated Clinical Research Coordinator to support their ongoing research initiatives in Welkom . This hybrid position requires a balance of on-site patient interaction and data management, with opportunities for remote administrative tasks. You will play a crucial role in the successful execution of clinical trials, ensuring compliance with protocols and regulatory standards. This role is vital for patient safety and data integrity, contributing directly to the advancement of new medical treatments. The ideal candidate possesses excellent communication skills and a thorough understanding of clinical trial processes.

Key Responsibilities

• Coordinate the day-to-day operations of clinical trials, ensuring adherence to study protocols and regulatory guidelines (e.g., ICH-GCP).
• Recruit, screen, and enroll eligible participants for clinical studies.
• Collect, process, and manage clinical data accurately and efficiently, including source document verification.
• Schedule participant visits, tests, and procedures, maintaining meticulous records.
• Serve as a liaison between investigators, study participants, sponsors, and regulatory agencies.
• Monitor patient safety and report any adverse events according to protocol requirements.

Requirements

• Bachelor's degree in a relevant healthcare or scientific field.
• Proven experience working in clinical research settings.
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
• Excellent organizational, time management, and multitasking abilities.
• Proficiency in electronic data capture (EDC) systems and medical terminology.
• Exceptional interpersonal and communication skills, with the ability to interact empathetically with patients.

Benefits

• Competitive salary and potential for performance bonuses.
• Comprehensive health, dental, and vision insurance.
• Paid time off and sick leave benefits.
• Professional development opportunities, including training and certifications.
• Exposure to innovative clinical research and therapeutic areas.
• Flexible hybrid work schedule to promote work-life balance.