Job Description

Clinical Trial Associate

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The Clinical Trial Associate provides administrative support to the clinical research teams in the full spectrum of the research activities such as pre-clinical research, study start-up, study management and site closure.

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Clinical research associates help to organize and monitor the different phases of clinical trials. Key responsibilities include:

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Responsibilities And Duties:

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- To assist Project Manager and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
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- To assist the clinical team in preparing, handling, distributing, filing, and archiving clinical documentation and reports according to the scope of work and standard operating procedures.
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- To assist with periodic review of study files for accuracy and completeness.
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- To assist with the tracking and managing Case Report Forms (CRFs), queries and clinical data flow.
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- To process Data Collection Forms, i.e. login, tracking,



quality control as appropriate for the study.
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- To assist in preparing Quality management system documentation and preparation for audits.
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- To provide general administrative support to the Clinical Operations Department.
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- To assist the Clinical teams in the completion of all required tasks to meet departmental and project goals.
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- To set up, organize and maintain clinical study documentation (e.g. Main Study Files, CRFs, etc.), including preparation for internal/external audits, final reconciliation and archival.
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- To assist in the coordination of Investigator payments, if applicable.
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- To assist in producing slides, overheads, etc., as needed for the project, departmental, sponsor and business development presentations.
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Qualifications:

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- equivalent experience degree in Clinical Background.
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- 2-3 year skilled Clinical Background experience
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- Excellent oral and

📌 Clinical Trial Associate (Surat)
🏢 Concept Medical
📍 Surat