Job Description
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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Job Overview
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Company
Hubforjobs Recruitments
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Experience
2+ years
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Location
Lagos
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Offered Salary
NGN150,000 - 250,000 Monthly
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Qualification
Degree
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Industry
Education, Teaching, Training
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Date Posted
December 02, 2024
Job location
Hubforjobs Recruitments
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Category
Consulting, Recruitment, HR Services
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Website
hubforjobs.com
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Location
Lagos, Nigeria