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PPD Clinical Trail Coordinator Openings for Freshers & Experienced

CLINICAL TRIAL COORDINATOR Fresher & Experience Job Openings at Bangalore Location. Educational Qualification, Experience, Job Description and More Information Check Below

Job Qualification

High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor’s degree preferred.

Previous experience that provides the knowledge, skills, and abilities to perform the job

Experience : comparable to Freshers (0) to 1 year.

JOB DESCRIPTION

  • Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization’s WPD and department guidance document.
  • According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
  • Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
  • Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads.
  • Supports the maintenance of study specific documentation and systems including but not limited to: study team lists, tracking of project specific training requirements, system access management, and tracking of project level activity plans in appropriate system.
  • Provides system support (i.e. GoBalto & eTMF). Supports RBM activities.
  • Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
  • Supports scheduling of client and/or internal meetings. Reviews and tracks local regulatory documents. Transmits documents to client and centralized IRB/IEC.
  • Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation. Maintains vendor trackers.
  • Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites. Assists with study-specific translation materials and translation QC upon request.

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