**Clinical Operations Statistician - Contract Role in Europe**
Are you a seasoned Clinical Operations Statistician looking for your next challenge? We are on the hunt for an individual with exceptional expertise and a minimum of 10 year's experience within late phase or phase 4 studies. This is a freelance, contract position where you will play an integral role dedicated to a sponsor, supporting performance by monitoring the clinical research organisations work load (CROs) through pivotal stages such as data base lock and ensuring secure storage of critical trial data.
Key Responsibilities:
- Work closely with CRO staff to prepare databases for locks
- Handle complex statistical analyses during various study phases
- Manage the organisation and long-term storage of clinical trial data
Required Skills:
- **Late Phase/Phase 4 Studies Expertise:** Your extensive background working on later stage trials provides assurance that our high standards can be met.
- **Data Base Lock Proficiency:** You'll bring proven ability to support teams up until database lock-an essential milestone marking readiness for regulatory submission.
- **Bio-statistics Knowledge:** As standard practice dictates, being well-acquainted with bio-statistical methods puts forth efficiency when dealing with intricate data sets.
This opportunity requires someone based anywhere across Europe who relishes freelancing flexibility while engaging deeply within their field. If this speaks directly to your professional aspirations, we invite applications from those prepared to elevate operations statistics into new realms of excellence within pharmaceuticals and clinical trials sectors.
