Description
Job Requirements:- Degree in Life Sciences with 7+ years in the pharmaceutical industry or in a CRO, including 2+ years' document preparation and writing experience. Preference will be given to candidates who have a degree in nursing, pharmacy or have a PhD or other advanced degree.
- Ability to assimilate technical and scientific information and proficient at data interpretation
- Knowledge of clinical trial design and basic statistics.
- Experience writing all types of clinical & regulatory documents and familiarity with registration dossiers for
worldwide use.
- Familiarity with requirements for regulatory submissions
- Has used 1 or more EDM systems
The position offers opportunity for advancement over time with responsibilities weighted towards a leadership role for study planning, oversight and conduct.
Please send over an updated CV to be considered