Clinical Research Coordinator
The GeneLab Bioscience Limited
Research, Teaching & Training
Healthcare
NGN
150,000 - 250,000
Easy Apply
New
1 week ago
Job Summary
We are looking to hire a Clinical Research Coordinator (CRC) who 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.
- Minimum Qualification : Degree
- Experience Level : Entry level
- Experience Length : 2 years
Job Description/Requirements
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
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.
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