Maria Gavides
Empower Your Clinical Research Site
I help physicians and medical practices establish, manage, and optimize their clinical research programs.
ABOUT ME
I am a Medical Doctor (MD), a graduate of Universidad Central de Venezuela (UCV), with over 5 years of clinical experience and more than 3 years of experience in clinical research in the United States.As the founder of Prime Trial Research Services, I help physicians and research sites establish, organize, and strengthen their clinical research programs.My experience includes clinical trial operations management across Phase I–III studies, from study activation through closeout, with a focus on pulmonology, dermatology, and internal medicine.I provide clinical research consulting, operations management, and remote operational support in English and Spanish.
Professional BackgroundMedical Doctor (MD)
Universidad Central de Venezuela (UCV)3+ Years
Clinical Research Experience5+ Years
Clinical ExperiencePhase I–III Clinical Trials
From Study Activation to CloseoutTherapeutic Areas
Pulmonology, Dermatology & Internal Medicine
SOLUTIONS FOR YOUR CLINICAL RESEARCH SITE
Managing multiple clinical trials, patients, vendors, and regulatory requirements can be challenging, especially without well-defined operational processes.At Prime Trial Research Services, we help clinical research sites identify areas for improvement, streamline operations, and establish efficient workflows.From study start-up and regulatory management to patient recruitment oversight and quality control, we provide practical solutions to strengthen your site's operations and overall performance.
MIS SERVICIOS
1. Clinical Research Site Readiness & Study Start-UpSite readiness assessments, development of operational workflows, essential documentation, and support with clinical trial activation.2. Regulatory Management & Quality ControlOrganization and maintenance of Investigator Site Files (ISF), coordination of regulatory documentation and IRB submissions, document review, and support with Good Clinical Practice (GCP) compliance.3. Clinical Research Operations Management & OptimizationOversight of patient recruitment and screening activities, workflow optimization, and remote operational support for clinical research sites.
LET'S TALK ABOUT YOUR CLINICAL RESEARCH SITEAre you looking to start conducting clinical trials or improve your site's operations?Let's discuss your needs and how I can help you build a more organized, efficient, and trial-ready clinical research program.
Email: [email protected]CONNECT WITH ME ON SOCIAL MEDIAI share educational content, professional insights, and practical tips about clinical research.LinkedIn: Maria GavidesInstagram: @mariagavidesresearch