When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel are currently recruiting a Trial Master File (TMF) specialist. This role can be based in Poland, Czech Republic, Hungary, Spain or South Africa.
In this role, the TMF Specialist works closely with Business & Technology Capabilities colleagues to support cross functional clinical study teams to maintain a complete and contemporaneous and high quality TMF. The TMF Specialist will demonstrate a good understanding of TMF processes and awareness of evolving regulatory requirements related to records management to support the development and delivery of TMF Operations strategy.
Perform Quality control activities process for TMF submissions to Veeva Vault (VV) eTMF in accordance with the documented process.
Carry out required activities in VV eTMF for all Clinical Vault/eTMF user access requests in accordance with the documented process.
Carry out required activities in VV eTMF for all requests for changes to be made to TMF documents in accordance with the documented process.
Member of the TMF Ops team that oversees the TMF Ops mailbox for all new TMF specific questions and requests, ensuring all requests are triaged to appropriate TMF Ops team members.
Support the development of study-specific, cross-departmental TMF Plans and TMF Indexes.
Support TMF health activities at a global level including generating TMF-relevant metrics from the eTMF system and escalating as necessary.
Support the development and delivery of a high standard training for the eTMF system and documented TMF process.
Support TMF process improvement activities as required.
Promote the use of VV eTMF with cross functional teams by building strong professional relationships and networks among peers and colleagues.
Support TMF Ops team activities in required TMF preparation for internal audits and/or Regulatory inspections.
Assist in mentoring and training new staff and contractors as relevant to their role.
Support any other Business & Technology Capabilities project activities as required.
Supports multiple TMF Operations activities and projects and will identify issues and escalate as needed to TMF Ops leads, promoting TMF inspection readiness and TMF best practices.
For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart.
Quality driven with a focus on attention to detail.
Flexible and adaptable to a fast-changing environment.
Good time management and organizational skills.
Strong IT skills (Microsoft Office suite, SharePoint).
Ability to work independently and in a global team environment to support overarching TMF Ops team deliverables.
Experience working in a TMF environment in a pharmaceutical company or CRO.
Current knowledge of Trial Master File Regulations and TMF Reference Model.
Previous experience working in an eTMF system (preferably Veeva Clinical Vault) as an end user, business, or system administrator.
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
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Originally posted on Himalayas
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