Clinical Research Associate

Clinical Research Associate (CRA) - Law ***** Art. 18Join to apply for theClinical Research Associate (CRA) - Law ***** Art. 18role atMedpaceClinical Research Associate (CRA) - Law ***** Art. 18Join to apply for theClinical Research Associate (CRA) - Law ***** Art. 18role atMedpaceOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Research Associate (law ***** Art. 18) to join our Clinical Monitoring team in Italy.This position will work with a team to accomplish tasks and projects that are instrumental to the company's success.If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.Medpace will provide comprehensive initial and ongoing training depending on your previous experience.ResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;Verification that the investigator is enrolling only eligible subjects;Regulatory document review;Medical device and/or investigational product/drug accountability and inventory;Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; andCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.QualificationsMaster degree in health-related field;Willing to travel *****% nationally;Familiarity with Microsoft Office;CRA certification completed as per DMC *************;Previous experience as CRA;Fluent in English and Italian language;Strong communication and presentation skills a plus.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People.Purpose.Passion.Make a Difference Tomorrow.Join Us Today.The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.The work we do today will improve the lives of people living with illness and disease in the future.Medpace PerksFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and ****Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/VetsSeniority levelSeniority level Not ApplicableEmployment typeEmployment type Full-timeJob functionJob function Research, Analyst, and Information TechnologyIndustries Pharmaceutical ManufacturingReferrals increase your chances of interviewing at Medpace by 2xGet notified about new Clinical Research Associate jobs inMilan, Lombardy, Italy .Clinical Project Coordinator - Entry LevelClinical trial start up Specialist - Area No ProfitClinical trial start up Specialist - Area ProfitExperienced Clinical Research Associate (CRA)Associate Clinical Trial Manager (PhD) - Infectious Disease / ImmunologyGreater Milan Metropolitan Area 10 hours agoAssociate Clinical Trial Manager (PhD) - Neuroscience / OphthalmologyNorthern Italy CRC II Onsite (Per diem, Part, Full time)Southern Italy CRC II Onsite (Per diem, Part, Full time)Sponsor Dedicated CRA II/Sr CRA - Home Based ITAClinical Science Associate Transplant - North East ItalySponsor Dedicated CRA II/Sr CRA I - Home Based ITAExperienced CRA, Sponsor Dedicated - Italy(Associate) Medical Director - NeurologyCMC RA Senior Manager/AD China submissionsWe're unlocking community knowledge in a new way.Experts add insights directly into each article, started with the help of AI.#J-*****-Ljbffr