Bilingual Clinical Research Associate

Il y a 5 heures

belgium belgium XPER Research Temps plein

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pstrongCRA (fluency in English and French) – based in Belgium /strong /ppDo you recognize yourself in below Skills Competences: /pulliClinical Trial Knowledge: Clear understanding of study designs, operational processes and regulations. /liliCommunication

Skills:
Clear, professional and collaborative interaction with cross-functional teams, investigators and sponsors. /liliProblem-Solving Decision-Making: Proficient in identifying issues and making data-driven decisions. /liliRelationship Building Teamwork: Strong at building partnerships with stakeholders and fostering collaboration across diverse teams. /liliAdaptability Attention to Detail: Flexible in dynamic environments while ensuring compliance. /liliTime Management Prioritization: Skilled in managing multiple studies, meeting deadlines and adapt to shifting priorities and competing demands. /liliSelf-Motivated Independent Worker: Effective in independently managing site activities, monitoring responsibilities and ensuring adherence to protocols and timelines. /li /ulpstrongI /strongn this role, you will have the opportunity to: /pulliAct as responsible person managing clinical study sites across various phases of the clinical study. /liliConduct qualification visits, site initiation visits, interim monitoring visits and close out visits to ensure adherence to study protocols, monitoring plans and applicable other study plans and manuals, applicable standard operating procedures and relevant regulations. /liliCommunicate regularly with investigators and site staff to provide guidance, support and training about study-related matters to ensure compliance /liliReview and resolve data queries and discrepancies in collaboration with site staff and data management teams. /liliCollaborate with site staff for proper reporting and follow-up of safety events, ensuring timely handling of safety issues. /liliIdentify and escalate protocol deviations, non-compliance issues and other risks to study integrity and subject safety as well as proactively address study-related issues and finds the appropriate solutions independently or in cooperation with project lead or project manager. /liliManage study supplies and oversee device accountability at sites. /liliFacilitate communication and collaboration between study sites and other stakeholders, such as sponsor team, CROs, vendors and ethics committees. /liliInteract with vendors as necessary. /liliActively participate in study team meetings. /li /ulpThe essential requirements of the job include: /pulliBased in Belgium /liliA Master of Science in a scientific, biological or medical science field /liliMinimum of 1-2 years’ experience in clinical research or equivalent by education or relevant experience /liliStrong experience using Microsoft applications (Excel, Word, PowerPoint, Outlook) /liliProficient in French and English – other languages are a plus /li /ulh3Ready to make an bIMPACT /b? /h3pWant to make a difference in clinical research? Apply via the button below, or send your CV and cover letter to /p

Bilingual Clinical Research Associate

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Bilingual Clinical Research Associate

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Emplois similaires à belgium belgium

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