- Experience Level
- Experienced (non-manager)
One of our specialist Pharmaceutical clients are seeking a CTA who has experience with the oversight of the eTMF to join them on an initial 12-month contract. They have seeking an individual with at least two years experience who can be the primary support for the eTMF and organisation of key documents.
Key responsibilities shall include:
Oversight and management of the eTMF
Experience of working on Veeva eTMF
Organising and maintaining the TMFs
Sponsor oversight files: collation of documents from monitors and/or CROs
Assist in setting up clinical study files
Create drafts of study specific documents.
Seek signatures for approved documents.
Support Clinical Project Managers
Arranging cross-functional meetings and distributing minutes
Assist with the tracking of project timelines
Maintain budget tracking tools when required
2+ years experience as CTA
Experience within a pharma/CRO environment
Knowledge of regulatory documents or terminology
Exposure to timeline and budget tracking
Experience with eTMF is essential.
Able to multitask and prioritise tasks
Good communication skills
If this position is of interest to you then please apply, or send your CV to email@example.com who is managing this role.
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