TMF Reviewer

When our values align, there's no limit to what we can achieve.
 

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)

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