Vacature detail

Junior Clinical Research Associate (Junior CRA)
Oxford Global Resources
Do you have a scientific background and have you had a first taste or want to work in the pharmaceutical/medical device industry ? Are you triggered to find out more about the development of new treatments for patients and orient your career in this direction ? Then check out the below, we are actively looking for enthusiastic Clinical Research Associate (CRA) candidates, motivated and eager to dive in and further explore the world of clinical research."Job DescriptionAs a CRA you plan, execute, and support clinical site management activitiesYou ensure the quality and integrity of the data collected in the client sponsored clinical trialsResponsibilities:Evaluate, initiate, monitor & close out clinical trial sites.Ensure site compliance and data qualityRespond to site-related queries and escalates issuesResponsible for operational site managementActively contribute to department results and goalsKey Activities:Develop site visit plans, conduct Clinical Site Evaluation, Initiation, Monitoring and Close Out visits and prepare visit reports for project manager review and approval.Build and maintain solid and long-term professional relationships with investigators and site staffFacilitate subject enrolment at the site level with focused patient recruitment strategies and action plansAssist in preparing sites for audits, review audit reports and contribute to resolving findingsIdentify site needs and site-related issues, escalate and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial processEnsure appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAES)Verify case reports and source documentationProvide input into case report forms and study-related documents as requestedPerform investigational product accountability and reconciliation.Maintain site study suppliesFacilitate the resolution of clinical queries to investigative staffProvide input into feasibility and identify clinical investigatorsEnsure clinical study sites are conducting the clinical trials in compliance with the respective protocol, SOPs and applicable ICH/GCP guidelines and regulationsRequirements:Bachelor or Master in sciencesFirst relevant experience (internship or industry)Very good knowledge of Dutch, French and EnglishGood working knowledge of common software packagesAttention to detailGood organizational skillsRelationship building skillsFlexibilityGood communication skillsPresentation skillsExisting right to work in EuropeBenefits Indefinite contract with a balanced salary package based on your capabilities and experience, including extra legal benefits.Vacancy number: 18829
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Heel Belgiƫ / toute la Belgique, null
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