Clinical Research Coordinator

Placements24; Pretoria; Hybrid; ZAR 320,000 - 420,000; Full time

Benefits offered by this job

Hybrid work arrangement

Professional development

Competitive salary

Job summary

Placements24 is seeking a meticulous Clinical Research Coordinator to support a busy clinical research unit in Pretoria. The role involves coordinating recruitment, data collection, and regulatory documentation, with a hybrid work model between on-site and administrative tasks.

Ideal candidates have a health-science background, at least two years of CRC experience, and strong knowledge of GCP and regulatory affairs.

Qualifications

• Bachelor's degree in a health science, nursing, or related field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar role.
• Thorough understanding of clinical trial processes, GCP, and regulatory affairs.
• Excellent organizational, time management, and communication skills.
• Proficiency in electronic data capture (EDC) systems and general office software.
• Ability to work independently and manage multiple priorities effectively in a hybrid work setting.

Responsibilities

• Recruit, screen, and enroll eligible participants for clinical trials according to study protocols.
• Schedule and coordinate participant visits, ensuring all study procedures are completed accurately.
• Collect, manage, and maintain accurate clinical trial data and source documentation.
• Ensure compliance with Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
• Liaise with investigators, study sponsors, and regulatory authorities as needed.
• Prepare study-related reports and maintain study master files.

Skills

GCP knowledge

Regulatory affairs

EDC (Electronic Data Capture)

Time management

Communication skills

Independent work

Education

Bachelor's degree in health science or related field

Job description

About the Role

Our client is seeking a meticulous and organized Clinical Research Coordinator to join their busy clinical research unit in Pretoria . This vital role supports the smooth execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for managing participant recruitment, data collection, and regulatory documentation, working closely with physicians, study participants, and pharmaceutical sponsors. This position offers a hybrid work model, allowing for flexibility between on-site coordination and remote administrative tasks. It's a great opportunity to contribute to advancing medical treatments and patient care within a dynamic research setting in Pretoria .

Key Responsibilities

• Recruit, screen, and enroll eligible participants for clinical trials according to study protocols.
• Schedule and coordinate participant visits, ensuring all study procedures are completed accurately.
• Collect, manage, and maintain accurate clinical trial data and source documentation.
• Ensure compliance with Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
• Liaise with investigators, study sponsors, and regulatory authorities as needed.
• Prepare study-related reports and maintain study master files.

Requirements

• Bachelor's degree in a health science, nursing, or related field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar role.
• Thorough understanding of clinical trial processes, GCP, and regulatory affairs.
• Excellent organizational, time management, and communication skills.
• Proficiency in electronic data capture (EDC) systems and general office software.
• Ability to work independently and manage multiple priorities effectively in a hybrid work setting.

Benefits

• Competitive salary and performance-based incentives.
• Comprehensive medical and retirement benefits.
• Opportunities for professional development and certifications in clinical research.
• Hybrid work arrangement offering flexibility.
• Engaging work environment focused on improving patient health outcomes in Pretoria .