Clinical Research Associate

hace 19 horas


Barcelona, España Medpace A tiempo completo

Clinical Research Associate - BarcelonaWe are seeking a full‑time, home‑based Clinical Research Associate located in Barcelona and surrounding areas.Medpace OverviewMedpace is a full‑service clinical contract research organization (CRO) providing Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Headquartered in Cincinnati, Ohio, we employ more than 5,000 people in 40+ countries.PACE (Medpace CRA Training Program)No clinical experience is required. The PACE training program will develop your CRA skills through interactive discussions, hands‑on exercises, and core rotations.Unexpected RewardsDynamic working environment with varying day‑to‑day responsibilitiesExpansive experience in multiple therapeutic areasTeam of therapeutic and regulatory expertsDefined growth ladder with mentoring and management opportunitiesCompetitive pay and travel bonus potentialResponsibilitiesConduct qualification, initiation, monitoring, and close‑out visits for research sites in compliance with approved protocol.Communicate with the medical site staff, including coordinators, clinical research physicians, and their teams.Verify adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff.Verify medical records and source documentation against case report form data, identify and report entry errors, and communicate protocol deviations per SOPs, GCP and applicable regulatory requirements.Verify investigator enrollment of eligible subjects.Review regulatory documents.Manage medical device / investigational product / drug accountability and inventory.Review adverse events, serious adverse events, concomitant medications and illnesses for accurate data reporting per protocol.Assess site recruitment and retention success and provide suggestions for improvement.Complete monitoring reports and follow‑up letters, summarizing findings, deviations, deficiencies, and recommended actions.QualificationsUniversity degree in a health or life science related field.Minimum 1 year of experience as a Study Coordinator, Clinical Research Coordinator, or CRA trainee.Approximately 60‑80% travel.Proficient knowledge of Microsoft Office and general computer literacy.Outstanding communication and presentation skills.Detail‑oriented with efficient time management.Excellent verbal and written communication skills in English and Spanish.Fluency in Catalan considered an asset.BenefitsFlexible work environment.Competitive compensation and benefits package.Competitive PTO packages.Structured career paths and professional growth opportunities.Company‑sponsored employee appreciation events.Employee health and wellness initiatives.AwardsRecognized by Forbes as one of America's Most Successful Midsize Companies (2021‑2024).Continually recognized with CRO Leadership Awards from Life Science Leader magazine.What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.#J-18808-Ljbffr



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