Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Hardworking and passionate job seeker with strong organizational skills eager to secure entry-level position. Ready to help team achieve company goals.
Overview
2
2
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Neomics Research Foundation
03.2022 - 03.2024
Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
Gathered, processed, and shipped lab specimens.
Collected data and followed research protocols, operations manuals, and case report form requirements.
Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
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