Clinical Research Coordinator (CRC)

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

Benefits offered by this job

Competitive salary

Professional development

Supportive team environment

Exposure to diverse therapeutic areas

Job summary

Placements24 is seeking a highly organized Clinical Research Coordinator (CRC) to support clinical trials in the Upington area. You will manage day-to-day study activities, ensure protocol integrity, and maintain patient data quality.

The role requires a minimum of 2 years' CRC experience, knowledge of GCP/ICH, and proficiency with CTMS/EDC systems. You will collaborate with physicians, patients, and sponsors in a fast-paced, team-oriented environment.

Qualifications

• High school diploma required; Bachelor's degree in health science preferred.
• Minimum 2 years of experience as a CRC or similar clinical research support role.

Responsibilities

• Recruit, screen, and enroll eligible participants into clinical trials according to protocol requirements.
• Schedule patient visits and conduct study procedures and questionnaires.
• Collect, process, and manage study data accurately in EDC systems.
• Maintain comprehensive study documentation and ensure GCP/ICH compliance.
• Monitor participants for adverse events and report as required.
• Assist investigators in preparing for site visits and audits.
• Collaborate with the clinical research team to ensure study timelines are met.

Skills

Organizational skills

Time management

Communication

Team collaboration

Education

Bachelor's degree in Health Science

High school diploma

Tools

CTMS

EDC software

Job description

About the Role

Our client is seeking a highly organized Clinical Research Coordinator (CRC) to support clinical trials in the Upington area. As a CRC, you will play a vital role in the day-to-day management of clinical studies, ensuring the smooth execution of protocols and maintaining the integrity of patient data. You will work closely with physicians, patients, and study sponsors to facilitate all aspects of research participation, from patient recruitment and screening to data collection and follow-up. This role is essential for advancing medical knowledge and bringing new therapies to patients.

Key Responsibilities

• Recruit, screen, and enroll eligible participants into clinical trials according to protocol requirements.
• Schedule patient visits, conduct study-related procedures, and administer questionnaires or case report forms.
• Collect, process, and manage study data accurately and confidentially in electronic data capture (EDC) systems.
• Maintain comprehensive study documentation and ensure compliance with regulatory guidelines (GCP, ICH).
• Monitor participants for adverse events and report them promptly as required.
• Assist investigators in preparing for site visits and audits from sponsors or regulatory authorities.
• Collaborate with the clinical research team to ensure study timelines are met.

Requirements

• High school diploma required; Bachelor's degree in a health science field is preferred.
• Minimum of 2 years of experience working as a CRC or in a similar clinical research support role.
• Solid understanding of Good Clinical Practice (GCP) and human subject protection principles.
• Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) software.
• Excellent organizational, time management, and communication skills.
• Ability to work effectively within a team and interact professionally with patients.

Benefits

• Competitive annual salary and comprehensive benefits package.
• Opportunities for professional development and certification in clinical research.
• Supportive work environment with experienced clinical research professionals.
• Contribution to groundbreaking medical research.
• Exposure to various therapeutic areas and clinical trial methodologies.