Clinical Research Coordinator

Placements24; Soweto; Hybrid; ZAR 240,000 - 420,000; Full time

Benefits offered by this job

Fully remote work arrangement

Health, dental & vision insurance

Professional development opportunities

Job summary

Placements24 seeks a highly organized Clinical Research Coordinator to join a fully remote clinical operations team. You will manage study documentation, coordinate patient visits, collect data, and liaise with investigators, sponsors, and regulatory bodies to ensure trial integrity.

The role emphasizes adherence to GCP, regulatory standards, and high-quality data collection, with remote collaboration across diverse stakeholders and globally impacting studies.

Qualifications

• Bachelor's degree in health or life sciences.
• At least 2 years' experience as a Clinical Research Coordinator or similar.
• Thorough knowledge of GCP and regulatory requirements.
• Experience with EDC systems and CTMS.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials, ensuring compliance with GCP and study protocols.
• Recruit, screen, and enroll eligible participants into clinical studies.
• Schedule and conduct patient visits, administer study procedures, and collect data.
• Maintain comprehensive study documentation, including source documents, CRFs, and regulatory files.
• Primary point of contact for investigators, study team members, sponsors, and IRBs/Ethics Committees.
• Monitor study progress, identify and resolve issues, and report study status to management.

Skills

Organizational skills

Time management

Multitasking

Communication skills

Interpersonal skills

Remote collaboration

Education

Bachelor's degree in health or life sciences

Tools

EDC systems

Clinical trial management software

Job description

About the Role

Our client is seeking a highly organized and dedicated Clinical Research Coordinator to join their fully remote clinical operations team. This role is vital for the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will manage study documentation, coordinate patient visits, collect data, and communicate with investigators, sponsors, and regulatory bodies. This position offers a unique opportunity to contribute to medical advancements from a remote setting, ensuring the integrity and efficiency of clinical research studies impacting patient care globally.

Key Responsibilities

• Coordinate and manage all aspects of assigned clinical trials, ensuring compliance with GCP and study protocols.
• Recruit, screen, and enroll eligible participants into clinical studies.
• Schedule and conduct patient visits, administer study procedures, and collect and manage trial data accurately.
• Maintain comprehensive study documentation, including source documents, case report forms (CRFs), and regulatory files.
• Serve as the primary point of contact for investigators, study team members, sponsors, and IRBs/Ethics Committees.
• Monitor study progress, identify and resolve issues, and report study status to management.

Requirements

• Bachelor's degree in a health science, life science, or related field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or similar role.
• Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proficiency in electronic data capture (EDC) systems and clinical trial management software.
• Excellent organizational, time management, and multitasking skills.
• Strong communication and interpersonal skills, essential for remote collaboration and interaction with diverse stakeholders.

Benefits

• Competitive salary commensurate with experience.
• Fully remote work arrangement, offering flexibility and work-life balance.
• Comprehensive health, dental, and vision insurance coverage.
• Opportunities for professional development and certification in clinical research.
• Contribution to impactful clinical trials that advance medical knowledge.
• A supportive and collaborative virtual team environment.