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.

How to Apply

Interested and qualified candidates should send their CV and Application Letter to: info@genelab.ng using the Job Title as the subject of the email.