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Clinical Research Support Specialist
Il y a 2 mois
Job Description
We are seeking a dedicated and organized Clinical Research Support Specialist to join our team at CENTRE HOSPITALIER UNIVERSITAIRE DE BORDEAUX. In this role, you will play a vital part in the smooth execution of clinical research projects focused on viral hepatitis.
- Your Responsibilities:
- Provide comprehensive logistical support for ongoing clinical research initiatives centered around viral hepatitis.
- Contribute to the meticulous planning and management of logistics for our annual congress, ensuring a seamless event experience.
- Offer backup assistance to active research protocols, maintaining project continuity and efficiency.
Key Activities:
- Actively participate in the research investigation process, contributing to data collection and analysis.
- Evaluate the feasibility of study logistics and develop associated cost estimates.
- Manage data/information effectively, ensuring accuracy, confidentiality, and accessibility.
- Serve as a reliable source of information and guidance for relevant stakeholders.
- Prepare biological samples for storage or shipment according to established protocols.
- Collect and analyze specific data/information, contributing to the generation of meaningful insights.
- Maintain meticulous documentation and ensure timely submission of required data.
- Monitor and follow up on adverse events, adhering to safety protocols and reporting procedures.
Additional Responsibilities:
- Supervise interns and new staff members in collaboration with the Clinical Studies Coordinator, fostering a supportive learning environment.
- Collaborate effectively with various hospital services to facilitate patient inclusion in research studies.
- Work closely with consultation, hospitalization, and diagnostic services to ensure seamless integration of research activities within the hospital setting.
Required Profile:
- Skills: Analyze patient medical records, build rapport with patients, evaluate data critically, maintain strict confidentiality, utilize specialized software applications proficiently.
- Knowledge: Scientific English fluency, database management expertise, proficiency in office tools, comprehensive understanding of medical ethics, familiarity with clinical research software, in-depth knowledge of internal hospital operations, thorough grasp of clinical research regulations, and strong command of medical terminology.
