Valerie Flores
Clinical Research Coordinator Iii @Houston Methodist
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WORK HISTORY
Clinical Research Coordinator Iii @Houston Methodist
Communicate directly with sponsors, CROs, IRBs, and trial participants and their families to conduct trial activities by monitoring participant safety, physician and investigator communications, and trial integrity. Collect data guided by FDA ICH-GCP as stipulated by federal and local regulations, institutional policies, and SOPs. Conduct all aspects of recruitment, consent, and retention of study subjects. Responsible for obtaining consent, reviewing trial eligibility, management of investigational products, laboratory processing and collection of vital signs, ECGs, spirometry, and phlebotomy. Oversee all components of a study required for successful completion of participant enrollment, safety monitoring, and retention from pre-study to close-out activities. Managing/ reviewing reconciliation of regulatory documents, IRB submissions, and financial tracking and billing in compliance with protocols and contracts. am in charge of negotiating clinical trial budgets and payment terms with sponsors
EDUCATION
The University of Texas Rio Grande Valley
Bachelor of Science - BS, Biology, General
University of Houston-Victoria
Master's degree, Biological and Biomedical Sciences
ABOUT VALERIE FLORES
Certified Clinical Research Professional. Experienced research coordinator with a…
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