Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives.
Analytical talents in project development and screening to document and report clinical study progress has consistently improved productively of research. Coordinates and facilitate research activities and submits protocols for regulatory approval. Serves as point-of-contact for clinical research professionals and coordinates lab samples to compile detailed data.