Clinical Trial Associate job in Bethesda at Technical Resources International
Technical Resources International

Job Info

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Responsibilities:

• Triage incoming emails, either as HelpDesk or other centralized/group email box.
• Process/track/distribute/upload designated clinical trial documents/artifacts, e.g., protocol deviations, site monitoring visit reports, essential regulatory documents (ERDs), etc. Generate/distribute Monthly/Quarterly reports regarding the documentation to internal and/or external stakeholders.
• Review information in centralized databases, e.g., patient recruitment/accrual, clinical data entered as EDC. Resolve queries, provide analysis assessments, and create/distribute periodic reports to internal and external stakeholders. Participate in centralized monitoring visits (CMVs).
• Provide Meeting/Webinar Support, i.e., distribute invites, track attendance, and complete/distribute meeting minutes/summaries to internal and external parties.
• Adherence to strict project timelines and expectations.
• Troubleshoot issues by applying existing knowledge to solve new problems.
• Create and maintain study specific contact lists.
• Assist with other operational activities when required, including tracking CRA visit schedules and visit statuses, and sending to internal or external stakeholders as directed.
• Reviewing, tracking, and managing study/project documents and filing as appropriate.
• Track progress of tasks and projects.
• Assist CRAs, CSMs, and/or In-House CRAs as needed.

Recommended Skills

• Irb
• Clinical Research
• Self Motivation
• Clinical Research Associate
• Clinical Trials
• Coordinating

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