Felicia Nica
Administrative Director, Clinical Research @UT MD Anderson
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WORK HISTORY
Administrative Director, Clinical Research @UT MD Anderson
Responsible for overseeing the conduct of a quality clinical research program, ensuring consistent adherence to good clinical practices, federal agency regulations, and institutional policies. Lead 150 clinical trial staff, support contract management, budget development, monitoring, regulatory compliance, and general day-to-day direction of the clinical research program.
EDUCATION
“Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
Doctor of Medicine (M.D.), General Medicine
The University of Texas Health Science Center at Houston (UTHealth)
Masters of Science (M.S.), Biomedical Sciences - Cancer Biology / Pharmacology
The University of Texas Health Science Center at Houston (UTHealth)
Graduate level courses, Clinical Research
Texas Woman's University
Executive MBA, Business Administration, Management and Operations
High-School for Mathematics and Physics No.4, Bucharest, Romania
Baccalaureat, Mathematics & Physics
ABOUT FELICIA NICA
Results-oriented and solutions-focused leader and team-player offering a unique blend of scientific, medical, regulatory, business and administrative backgrounds that combine to provide successful business strategies within complex drug and device development and clinical research areas. Demonstrated good decision making, leadership, and vision that work in concert to facilitate an environment that encourages excellence, cooperative cross-functional collaboration, and innovation. Strategic planning, administrative oversight, standard operating procedures development, regulatory compliance, operations, and Clinical Research protocols within the number one US cancer center and a world class academic medical center. Great ability to conceptualize and implement solutions while upholding the highest ethical and moral principles. Experience: Medical practice and scientific research • Oncology clinical trial management, FDA regulatory compliance, data and safety reporting for drug and device trials (INDs and IDEs) • Protocol review and development process • FDA interactions regarding clinical trial submissions and regulatory reporting • Clinical Trial Monitoring • Process improvement, data analysis, project management, strategic planning and handling multiple tasks concurrently and meeting deadlines despite conflicting demands • Supervising, mentoring, people leadership • Leading, liaising and coordinating cross-functional project teams • Management, finance and business practices concerning clinical research projects and programs • Business management/development and team leadership • Clinical research operations, budgets, grants, contracts • eCTD Certifications: Certified Clinical Research Professional (CCRP), Regulatory Affairs Certified (RAC-US), Certified IRB Professional (CIP) Skills and Abilities Attention to detail with a high priority for timely and accurate information. Ability to work independently, as well as on cross-functional and interdisciplinary teams. Strong time management/organizational skills. Strong verbal and written communication skills. Strong analytical and interpersonal skills. Ability to work under pressure and balance many competing priorities. Interaction with research teams and leadership in a professional manner. Management and leadership skills. Ability to think strategically and proactively with long term implications and impact. Willingness to always learn and improve processes. Perseverance in the face of challenges. High adaptability. Remote work skills.
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