María García López
Calle de los Olivos 24, 28002 Madrid, Spain
+34 91 445 8762
maria.garcia.lopez@email.com
https://www.linkedin.com/in/mariagarcialoneuroscience


PROFESSIONAL EXPERIENCE

Founder & CEO
NeuroVision Ibérica, Madrid, Spain
January 2020 – Present

Founded and lead a cognitive neuroscience research and educational corporation focused on advancing understanding of neural mechanisms underlying perception and cognition. Oversee all strategic initiatives, research operations, educational programming, and organizational development.

• Direct multidisciplinary research teams investigating cognitive neuroscience applications in clinical and educational settings
• Establish and maintain collaborative partnerships with academic institutions, healthcare organizations, and industry stakeholders
• Design and implement comprehensive educational programs and training curricula in neuroscience for diverse audiences
• Manage organizational budget, resource allocation, and operational infrastructure to ensure sustainable growth
• Develop and enforce ethical protocols and compliance standards for all research activities in accordance with institutional review board requirements
• Secure funding through grant writing, investor relations, and strategic partnerships, generating over $2M in research funding
• Mentor junior researchers and graduate students, fostering career development and scientific excellence
• Author scientific publications and deliver presentations at national and international conferences


Senior Medical Science Liaison
Therapeutics Innovación Europe, Barcelona, Spain
March 2017 – December 2019

Served as scientific expert and key opinion leader liaison for immunology therapeutic portfolio, bridging clinical research and medical affairs functions across multiple disease states.

• Established and maintained relationships with over 50 key opinion leaders in immunology, rheumatology, and gastroenterology
• Provided scientific support and education to healthcare professionals regarding mechanism of action, clinical trial data, and therapeutic applications
• Identified and communicated emerging scientific trends, competitive intelligence, and unmet medical needs to internal stakeholders
• Collaborated with clinical development teams to support investigator-initiated studies and clinical trial recruitment
• Delivered scientific presentations at medical conferences, advisory boards, and educational symposiums
• Ensured all activities maintained compliance with pharmaceutical industry regulations and company policies


Clinical Research Manager
Clínica Ensayos Clínicos, Valencia, Spain
June 2014 – February 2017

Managed multi-site clinical trials across oncology, endocrinology, and immunology therapeutic areas, ensuring protocol compliance and data integrity throughout study lifecycle.

• Oversaw clinical trial operations for 8 concurrent Phase II-IV studies with budgets exceeding $15M
• Supervised team of 6 clinical research associates and coordinators, providing training and performance management
• Implemented clinical trial management systems and standard operating procedures to optimize operational efficiency
• Conducted site selection, initiation, monitoring, and close-out activities in accordance with Good Clinical Practice guidelines
• Managed relationships with contract research organizations, institutional review boards, and regulatory agencies
• Prepared and reviewed clinical documentation including protocols, informed consent forms, and regulatory submissions
• Tracked study budgets, timelines, and deliverables, implementing corrective action plans when necessary


Clinical Research Coordinator
Grupo de Investigación Médica, Sevilla, Spain
August 2011 – May 2014

Coordinated clinical trial activities for neuroscience and pharmacology studies, ensuring adherence to protocol requirements and regulatory standards.

• Recruited, screened, and enrolled study participants while maintaining strict confidentiality and ethical standards
• Conducted study visits, administered assessments, and collected biological samples according to protocol specifications
• Maintained accurate and complete clinical trial documentation and regulatory files for audit readiness
• Managed investigational product accountability, storage, and distribution in compliance with pharmacy regulations
• Served as primary liaison between study participants, investigators, and sponsor representatives
• Entered and verified clinical data in electronic data capture systems with 99.8% accuracy rate
• Assisted with institutional review board submissions and correspondence


EDUCATION

Doctor of Philosophy (Ph.D.) in Neuroscience
Universidad Autónoma de Madrid, Madrid, Spain
September 2007 – May 2011

Dissertation: Neural Mechanisms of Sensory Integration and Perceptual Decision-Making

Master of Science (M.S.) in Molecular Biology
Universidad de Alcalá, Alcalá de Henares, Spain
September 2005 – June 2007

Bachelor of Science (B.S.) in Biology
Universidad Complutense de Madrid, Madrid, Spain
September 2001 – May 2005


SKILLS

Research & Scientific Expertise: Neuroscience, Clinical Research, Immunology, Oncology, Endocrinology, Pharmacology, Molecular Biology, Genomics, Proteomics, Medical Devices

Clinical Operations: Clinical Trials, Good Clinical Practice, Protocol Development, Clinical Trial Management Systems, Clinical Monitoring, Institutional Review Board, Clinical Documentation, Ethics, Audit

Leadership & Management: HR Management, Team Leadership, Mentoring, Training, Strategic Planning, Supply Management, Budget Management, Accountability

Communication & Collaboration: Presentation Skills, Public Relations, Writing, Reporting, Teamwork, Listening, Communication

Technical: Microsoft Excel, Microsoft Word, Information Management Systems, Data Entry, Documentation, Records Management

Professional Competencies: Investigation, Planning, Administration, Policies and Procedures, Confidentiality, Initiative, Customer Service