Role & Responsibilities
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Coordinate and manage clinical trials at site level
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Support patient screening, recruitment and follow-up
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Ensure compliance with protocol, GCP and regulatory guidelines
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Maintain accurate source documents and trial records
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Coordinate with investigators, CRAs, sponsors and ethics committees
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Support site initiation, monitoring visits and audits
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Manage study data and timely reporting
Qualification
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Bachelor’s degree in Life Sciences, Medical Sciences or related field
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OR Master’s degree in Life Sciences
Experience
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2–3 years of experience as a Clinical Research Coordinator
Skills
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Strong knowledge of clinical trial operations
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Good understanding of GCP and site management
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Excellent communication and documentation skills
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Good organizational and coordination abilities
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Attention to detail and compliance-driven approach
About the Company
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HRAPL is a clinical research organization focused on site management and trial execution
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Provides structured research support with strong compliance standards
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Offers long-term career growth in clinical research operation