Clinical Research Coordinator

Placements24; East London; On-site; ZAR 360,000 - 540,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Professional development

Supportive team

Diverse therapeutic areas

Job summary

Placements24 is seeking a Clinical Research Coordinator to support our East London clinical trials unit. You will coordinate activities, ensure protocol and regulatory compliance, and work with investigators and sponsors to facilitate trial operations.

The role emphasizes meticulous documentation, patient safety, and collaboration in a professional healthcare setting, with opportunities for professional development in clinical research methodologies.

Qualifications

• Bachelor's degree in a health-related field or equivalent experience.
• Experience as a Clinical Research Coordinator or in a related role.
• Strong understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
• Excellent organizational, communication, and interpersonal skills.
• Ability to work collaboratively in East London.

Responsibilities

• Coordinate all study-related activities for assigned clinical trials in adherence to protocols.
• Recruit, screen and enroll participants with informed consent.
• Manage study documentation and regulatory files, ensuring data accuracy.
• Monitor patient safety and report adverse events per guidelines.
• Liaise with investigators, sponsors, and regulators to ensure smooth trial operations.

Skills

Organizational skills

Communication skills

Interpersonal skills

ICH-GCP knowledge

Education

Bachelor's degree in a health-related field or equivalent experience

Job description

About the Role

Our client is seeking a highly organized and experienced Clinical Research Coordinator to join their dedicated clinical research unit in East London . This role is pivotal in supporting the execution of clinical trials, ensuring that studies are conducted according to protocol, regulatory requirements, and ethical standards. You will work closely with principal investigators, study participants, and study sponsors to facilitate all aspects of clinical trial management. This position is ideal for a detail-oriented individual committed to advancing medical knowledge and patient care through rigorous and compliant clinical research within a professional healthcare setting.

Key Responsibilities

• Coordinate all study-related activities for assigned clinical trials, ensuring adherence to protocols.
• Recruit, screen, and enroll study participants, ensuring informed consent is obtained.
• Manage study documentation, maintain regulatory files, and ensure data accuracy and completeness.
• Monitor patient safety and report adverse events promptly according to guidelines.
• Liaise with investigators, sponsors, and regulatory authorities to ensure smooth trial operations.

Requirements

• Bachelor's degree in a health-related field or equivalent experience.
• Previous experience as a Clinical Research Coordinator or in a related clinical research role.
• Strong understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple tasks efficiently and work collaboratively in a clinical research environment in East London .

Benefits

• Competitive salary and comprehensive benefits package.
• Opportunities to contribute to groundbreaking medical research.
• Professional development and training in clinical research methodologies.
• A supportive team environment focused on patient care and scientific integrity.
• Exposure to diverse therapeutic areas within clinical trials.