Posted 29 August, 2026
Clinical Trial Associate
Concept Medical
393050, GJ, IN
Full Time
Reference: ddd66ae2372ffee5
Job Description
Clinical Trial Associate
\nThe 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.
\nClinical research associates help to organize and monitor the different phases of clinical trials. Key responsibilities include:
\nResponsibilities And Duties:
\n- \n
- 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. \n
- 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. \n
- To assist with periodic review of study files for accuracy and completeness. \n
- To assist with the tracking and managing Case Report Forms (CRFs), queries and clinical data flow. \n
- To process Data Collection Forms, i.e. login, tracking, quality control as appropriate for the study. \n
- To assist in preparing Quality management system documentation and preparation for audits. \n
- To provide general administrative support to the Clinical Operations Department. \n
- To assist the Clinical teams in the completion of all required tasks to meet departmental and project goals. \n
- 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. \n
- To assist in the coordination of Investigator payments, if applicable. \n
- To assist in producing slides, overheads, etc., as needed for the project, departmental, sponsor and business development presentations. \n
Qualifications:
\n- \n
- equivalent experience degree in Clinical Background. \n
- 2-3 year professional Clinical Background experience \n
- Excellent oral and written communication skills, \n
- Professional in-depth knowledge of regulations in the Medical Device industry. \n