Clinical Associate III
- Central
- Contract
- Drug Safety / Pharmacovigilance
An exciting opportunity for an experienced Clinical Associate to work within a global pharmaceutical organisation.
Key Responsibilities include:
- Participating in the design, administration and monitoring of clinical trial.
- Analysing and evaluating clinical data gathered during research.
- Ensuring compliance with protocol and overall clinical objectives.
- Knowledge of FDA regulatory requirements is required.
The candidate must have the rights to work in the location stated in the job advert.
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