Clinical Research Coordinator (CRC) at Pomat Health Nigeria Limited

Pomat Health is a pioneering Clinical Research Organization (CRO) based in Nigeria, dedicated to accelerating healthcare innovation, and enhancing patient outcomes across Africa. We are on a mission to bridge the gap between clinical research and local communities.

We are recruiting to fill the position below:

Job Title: Clinical Research Coordinator (CRC)

Location: Yaba, Lagos
Employment Type: Full-time

Job Summary

• We seek a skilled Clinical Research Coordinator (CRC) to join our team. The Clinical Research Coordinator (CRC) will be responsible for managing day-to-day clinical trial activities, ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• The CRC will work closely with the Clinical Trial Manager, clinical sites, and study participants to ensure the successful implementation of research protocols, data collection, and patient safety measures.
• This position offers an opportunity to join a dynamic team committed to advancing clinical research in a fast-paced, supportive environment.

Key Responsibilities
Participant Recruitment & Consent:

• Patient Screening & Enrollment
• Participant Retention

Protocol Implementation & Compliance:

• Protocol Adherence
• Visit Coordination
• Informed Consent Documentation

Data Collection & Management:

• Source Documentation & Data Entry
• Query Resolution
• Sample Collection & Processing

Site Coordination & Communication:

• Site Support
• Documentation & Reporting
• Monitor Coordination

Regulatory & Compliance Support:

• Regulatory Documentation
• Audit Readiness
• Safety Monitoring

Participant and Site Education:

• Training Coordination

Job Requirements

• Bachelor's Degree in Nursing, Life Sciences, Health Sciences, or a related field. Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) is an asset.
• Minimum of 2 years of experience in clinical research, preferably in a CRO, clinical trial site, or healthcare setting.
• Knowledge of GCP, ICH guidelines, and regulatory standards applicable to clinical trials.
• Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.
• Excellent organizational, communication, and interpersonal skills, with a strong focus on participant safety and data accuracy.
• Experience in a start-up or fast-paced environment is a plus.
• Willingness to travel for site visits and participant follow-ups, if necessary.

Application Closing Date
30th December, 2024.