Clinical Research Monitor

Company DescriptionPSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionAs a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. We are committed to developing our employees in their careers by providing tailored courses and mentoring.You will:Conduct and report all types of onsite monitoring visitsBe involved in study startup and feasibility researchPerform CRF review, source document verification, and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressSupport the regulatory team in preparing documents for study submissionsQualifications:College/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experience in MexicoExperience in all types of monitoring visits in Phase II / IIIFull working proficiency in English and SpanishProficiency in MS Office applicationsAbility to plan and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelAdditional Information:This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.#J-18808-Ljbffr