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Research Nurse/Clinical Research Associate (CRA)

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 Research Nurse/Clinical Research Associate (CRA) plays a vital role in ensuring the integrity, compliance, and successful execution of clinical trials. This role involves rigorous site management, including monitoring, data verification, patient care, and protocol adherence, to ensure that clinical trials meet all regulatory, GCP, and protocol.

  • Minimum Qualification : Degree
  • Experience Level : Entry level
  • Experience Length : 3 years

Job Description/Requirements

Responsibilities:

  • Clinical Site Management & Compliance
  • Regulatory & Protocol Compliance
  • Informed Consent Verification
  • Monitoring Activities
  • Source Document Review & Data Verification
  • Protocol Deviations & Safety Monitoring
  • Investigational Product (IP) Management
  • Data Management & Query Resolution
  • Data Quality Oversight
  • Tracking & Documentation
  • Site & Project Coordination
  • Site Training & Delegation
  • Communication & Issue Resolution
  • Log & Equipment Verification
  • Site Audit Preparation & Support
  • Collaboration & Training
  • Training & Meeting Participation
  • Patient Recruitment & Retention
  • Escalation & Follow-Up



Requirements:

  • Bachelor’s degree in nursing, Life Sciences, Pharmacy, or related field. Registered Nurse (RN) certification is preferred.
  • Minimum of 3 years of experience as a Research Nurse, CRA, or similar role within a CRO, clinical trial site, or healthcare setting.
  • Strong knowledge of GCP, ICH guidelines, and other regulatory frameworks governing clinical research.
  • Proven experience in conducting site monitoring visits, data verification, and patient care within clinical trials.
  • Excellent communication, organizational, and problem-solving skills, with the ability to work independently and as part of a team.
  • Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.
  • Willingness to travel to clinical sites for monitoring visits, training, and site support.

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