Militza Vera de Alba

WORK HISTORY

EDUCATION

ABOUT MILITZA VERA DE ALBA

I have over 10 years’ progressive success executing critical, international drug trials and research programs for global pharmaceutical companies. My history includes directing 50+ clinical trials, and a record of securing regulatory and market approvals, delivering statistically significant results, minimizing outliers, and promoting patient/subject health and safety.Throughout my career, I’ve been frequently sough-after for my process development and improvement expertise. I’m able to rapidly assess the feasibility of proposed product development and clinical trial strategies, and present solutions to senior leadership teams.Notable accomplishments:Managed execution of up to 28 simultaneous trials.Developed and implemented health safety protocols, served as “informed consent” subject matter expert.Led multi-country clinical phase I, II, and trials.Identified cost-effective solutions and techniques; presented recommendations to CEO. Consistently promoted efficacy of results to avoid financial losses and maximize ROI.Met all study milestones by driving projects and communicating changes to country-level associates.Additionally, I have a talent for building and coaching high-performance teams. I frequently mentor employees to develop skill mastery and expertise. My Therapeutic expertise includes: Oncology, Diabetes, Men’s Health, Endocrinology, Immunology, Neurology, and Pediatrics.My practical experience is complemented by a Clinical Research Postgraduate Degree and a Medical Degree.I’m always happy to expand my professional network, please contact me here on LinkedIn or by email at: m••••••••@gmail.comSpecialities:Directing Clinical Trials & ResearchSecuring Regulatory & Market ApprovalsStrategic Planning & Risk MitigationClient Presentations & Product DemosMedical Affairs & ProcessesStudy Design & OptimizationContinuous Process ImprovementsManaging Global/International TeamsPharmacovigilance/Trial Monitoring