Soweto Clinical Research Coordinator | Trial Operations

Placements24; Soweto; Hybrid; ZAR 360,000 - 600,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

Job summary

Placements24 seeks a dedicated Clinical Research Coordinator for a role in Soweto, Gauteng. You will manage trial operations, recruit participants, and ensure data integrity while adhering to regulatory requirements.

The candidate should be organized, detail-oriented, and passionate about advancing medical research. You will work closely with investigators, study sponsors, and participants to ensure protocol compliance and patient safety, contributing to the successful execution of clinical

Qualifications

• Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field.
• Experience as a Clinical Research Coordinator or similar preferred.
• Strong understanding of clinical trial processes and GCP guidelines.
• Excellent organizational, time management, and multitasking skills.
• Proficient data entry and management with meticulous attention to detail.

Responsibilities

• Recruit, screen, and enroll eligible participants into clinical trials.
• Schedule and manage participant visits, ensuring protocol requirements are met.
• Administer study medication and conduct study procedures as directed by the investigator.
• Maintain accurate patient data and study records in line with regulatory standards (GCP).
• Monitor participants for adverse events and report them as required.
• Educate participants and families about the study protocol and expectations.
• Maintain communication with investigators, sponsors, and regulatory authorities.
• Ensure compliance with study protocols and institutional policies.

Skills

Regulatory knowledge

Data management

Communication

Organization

Team collaboration

Education

Bachelor's degree in Nursing/Life Sciences

Tools

EDC systems

Job description

Placements24 seeks a dedicated Clinical Research Coordinator for a role in Soweto, Gauteng. You will manage trial operations, recruit participants, and ensure data integrity while adhering to regulatory requirements.

The candidate should be organized, detail-oriented, and passionate about advancing medical research. You will work closely with investigators, study sponsors, and participants to ensure protocol compliance and patient safety, contributing to the successful execution of clinical