CK Group are recruiting for a Clinical Trial Administrator to join a company in the Pharmaceutical industry at their site based in Leeds on a contract basis for 12 months.
Hourly £14.19 per hour
Clinical Trial Administrator Role:
? Clinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload).
? Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions.
? Creation/distribution of regulatory binders and the wet-ink signed documents binder.
? Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions.
? Assist in providing internal communication of important clinical data and events.
? Minimum of a Bachelor?s Degree is required.
? Previous clinical research experience would be beneficial.
? Previous administrative support experience or equivalent for 1 year plus.
? Clinical/medical background would be advantageous.
? Experience and knowledge working with computer systems (Microsoft office ? Excel, Word and Power Point).
Our client is a multinational medical devices, pharmaceutical and consumer packaged goods manufacturing company who offer the worlds most comprehensive portfolio of orthopaedic and neuro products and services for joint reconstruction, trauma, spine, sports medicine, neuro, cranio-maxillofacial, power tools and biomaterials.
This Clinical Trial Administrator role will be based at our clients site in Leeds, Yorkshire.
Entitlement to work in the UK is essential. Please quote reference 50772.
You must be eligible to work in the UK. Learn more
- Agency: CK Group
- Contact: Julie Marshall
- Phone: 01438 723 500
- Reference: 50772
Website: CK Group
- Posted: 2nd June 2021
- Expires: 30th June 2021