Charo Fernandez De La Reguera Mantilla
About Charo Fernandez De La Reguera Mantilla
Charo Fernandez De La Reguera Mantilla is the Line Manager of Project Managers (STM) and CTAs (CTAs & CAs) at Bristol-Myers Squibb in Madrid, Spain. She has extensive experience in clinical trial management and a background in pharmacy and pharmaceutical industry studies.
Current Position at Bristol-Myers Squibb
Charo Fernandez De La Reguera Mantilla serves as the Line Manager of Project Managers (STM) and CTAs (CTAs & CAs) at Bristol-Myers Squibb. Based in Madrid y alrededores, España, she oversees project managers and clinical trial assistants, ensuring that projects align with the company’s operational standards and goals.
Experience at Covance for MSD
From 2015 to 2018, Charo worked at Covance as a Clinical Operation Manager and Line Manager on behalf of MSD. With a tenure spanning three years, she contributed to the clinical operations in Madrid y alrededores, España. Her responsibilities included managing clinical trials and directing operations to meet regulatory compliance and project objectives.
Role in Oncology Trials at Quintiles
In 2015, Charo held the position of Line Manager at Quintiles, working on oncology trials for Eli Lilly. She was involved in coordinating clinical trials across various European countries, including Spain, Hungary, Czech Republic, Slovakia, and Romania. Her role focused on ensuring the trials adhered to regulatory standards and were executed efficiently.
Clinical Trial Management at SGS Life Science Services
Charo has extensive experience in clinical trial management, notably having worked at SGS Life Science Services from 2001 to 2014. During her 13-year tenure, she managed numerous clinical trials, ensuring they met quality standards and regulatory requirements. Her role was critical in overseeing the clinical operations and facilitating smooth processes.
Educational Background and Certifications
Charo has a robust educational background. She earned her degree in Pharmacy from Licenciada en Farmacia and accomplished her Master in Industria Farmacéutica y Parafarmacéutica from C.E.S.I.F. Additionally, she obtained a PDD from the Escuela de Organización Industrial and achieved certification as an Auditor Jefe ISO 9001 from SGS. She also holds a qualification in Regulatory Affairs and Pharmacovigilance from ESAME.
Therapeutic Expertise and Leadership Style
Charo possesses extensive therapeutic expertise, managing clinical trials in areas such as Oncology, Infectious Diseases, Central Nervous System (CNS), Cardiovascular, Dermatology, Nephrology, Endocrinology, Pediatrics, Rheumatology, and Diabetes. Known for her soft leadership style, she fosters a collaborative atmosphere by integrating team and stakeholder perspectives. She emphasizes quality and simplicity in achieving goals within regulatory standards.