Clinical Trial Associate

Company: Concept Medical
Apply for the Clinical Trial Associate
Location: Surat
Job Description:

Clinical Trial Associate

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.

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

Responsibilities And Duties:

  • 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.
  • 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.
  • To assist with periodic review of study files for accuracy and completeness.
  • To assist with the tracking and managing Case Report Forms (CRFs), queries and clinical data flow.
  • To process Data Collection Forms, i.e. login, tracking, quality control as appropriate for the study.
  • To assist in preparing Quality management system documentation and preparation for audits.
  • To provide general administrative support to the Clinical Operations Department.
  • To assist the Clinical teams in the completion of all required tasks to meet departmental and project goals.
  • 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.
  • To assist in the coordination of Investigator payments, if applicable.
  • To assist in producing slides, overheads, etc., as needed for the project, departmental, sponsor and business development presentations.

Qualifications:

  • equivalent experience degree in Clinical Background.
  • 2-3 year professional Clinical Background experience
  • Excellent oral and written communication skills,
  • Professional in-depth knowledge of regulations in the Medical Device industry.

Posted: March 5th, 2026