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TMF Reviewer

India, Remote Job ID R0000017927 Category Clinical Trials
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About this Role

TMF Support

  • Collaborates with the TMF Inspection Readiness Specialist to plan and execute assigned tasks.
  • Maintains overview of the agreed planning, proactively providing status updates and notifying trends to the study team and TMF IR Specialist.
  • Stays flexible and always looks for proactive, responsible solutions to ensure client satisfaction.
  • Provides feed-back to PS/FL Super Users in CRS Technology in order to enable enhanced systems, tools and processes.

TMF Quality Management

  • Maintains the TMF for ongoing studies according to Parexel SOP’s or contractual obligation to sponsor, by performing completeness checks/ milestone reviews or other TMF contracted tasks according to the established timelines and quality criteria.
  • Proactively cooperates with LM and FLs on project’s TMF tasks.
  • Understands how their own role and expertise impact TMF quality and timeliness.

TMF Audit Support

  • Takes proactive measures to prepare study for audit.
  • Facilitates internal and external TMF audits.

Facilitate process and tool updates

  • Collaborate with the study team and manages TMF tools customization and TMF Plan / CFMP Development and sign off.

TMF Archival Preparation

  • Participates in the TMF closure process as required by Sponsor and Parexel Procedures.
  • Prepares eCRF CDs and participates in eCRF process as defined in the relevant manuals and SOPs

Competencies, skills and abilities:

  • Good computer skills including but not limited to the knowledge of Clinical Trial Systems, eTMF systems and MS-Office products such as Excel, Word
  • Data Processing and analysis skills, including management of TMF documents as per the process using different systems/tools for TMF Audit/Inspection readiness
  • Ensure effective, open, timely, and collaborative written and verbal communication, with internal and on occasion external stakeholders
  • Ability to successfully work in a (“virtual”) team environment: In-depth understanding of how the team integrates with others in accomplishing the objectives of the area
  • Able to demonstrate basic problem solving and risk management activities
  • Effective time management, prioritizing multiple tasks in order to meet daily metrics, team and project objectives
  • Proactive management of work quality and the assurance of consistent delivery of high-quality outcomes, minimizing wasted effort and maximizing positive results from performed work
  • Able to take initiative and work independently, seeking guidance only when necessary and escalating issues as required
  • Strong internal customer focus
  • Offering of support and constructive feedback to project team members
  • Exhibits a sense of urgency about solving problems and completing work

Knowledge and Experience:

  • Preferred experience with clinical trials, or managing documentation
  • Good understanding of procedures and concepts within own technical/subject area and a proficient knowledge in other related areas.
  • Prior experience in an international environment would be advisable.
  • Strong command of written and spoken English language

Education:

  • Bachelor’s degree preferred (or relevant clinical or business equivalent)                          

#LI-REMOTE
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