Clinical Research Coordinator Resume Profile

Confidential

Clinical Research Coordinator

Participate in clinical research studies conducted by the Principal Investigator.
Participate in a variety of complex activities involved in the collection, compilation, and documentation of clinical research data while adhering to ICH/GCP guidelines and Code of Federal Regulations.
Perform study specific regulatory processes across multiple studies of different therapeutic areas and phases, in accordance to appropriate regulations, SOPs, and study specific protocols.
Ensure timely and accurate transcription of information on source documents, paper case report forms
CRFs , and electronic CRFs.
Obtain blood samples, cultures, tissues and other specimens for laboratory analysis.
Specimen storage and shipment.
Perform ECGs.
Manage laboratory.
Recruit subjects for research studies.