Your “2 for 1” Team

Clinical Operations professional, 15+ years experience within CRO / Site / Sponsor / Advisory Board
In-depth therapeutic and medical knowledge, across dozens of therapeutic indications
Success across all phases of global clinical trials
Experienced in the dynamic environment of Biotech startups
Site Advocate and Speaker/Panelist for industry conferences
Mentioned in a recently published book titled “The Patient Recruitment Conundrum” by Ross Jackson
Specialization: process optimization, policy development, project planning and management, start-up/execution, 360-degree clinical trials operations expertise, budgeting, Sponsor-level selection and oversight obligations for Service Providers/CROs, vendor management, regulatory compliance, team leadership, and fostering collaboration amongst internal and external stakeholders

Clinical Research and Drug Development professional, 25+ years experience within CRO / Sponsor / Advisor / Consultant
Experienced developing pharmaceuticals, biologics, vaccines, and in vitro diagnostics (IVD); U.S. and global Phase I-IV human clinical trials
Therapeutic experience: Pain & Analgesia, CNS & Neurology, Infectious Disease, Cardiovascular Disease, Oncology & Hematology, Dermatology, Respiratory Disease, and Ophthalmology
Fully bilingual in English & Spanish; previously served as a member of the DIA Advisory Council of Latin America (ACLA)
As acting VP/Exec. Director of Clinical Operations for a small, clinical-stage pharmaceutical company, directly liaised with the U.S. FDA
Specialization: VP/Director-level Clinical Operations oversight, Alliance/Program management, Executive Steering & Operations Management Committees, clinical trials project management (strategy, design, staffing, execution), Service Provider/CRO selection and oversight management, budgets and contracts negotiation, clinical trials monitoring, clinical documents content development, Quality Improvement & Mentoring groups, and cross-functional team management & development