We are currently looking to recruit an experienced Clinical Research Associate.
The major tasks would be:
- Perform (co-)monitoring activities (initiation visits, monitoring visits, close out visits) according to the applicable SOPs and guidelines
- Study administration and financial control at site level
- Accurate reporting of study progress
- Ensure quality of data generated by managed sites for consistently low query levels
- Manages sites resulting in acceptable audit reports
- Maintain strong relationship with investigator and staff, resulting in investigator satisfaction and compliance
- Travels as necessary (up to 50% of the time), consistent with study needs
- Supports organization of and participates in study team and investigator meetings
Profile:
Degree in biomedical discipline or equivalent experience
Familiar with Good Clinical Practice (ICH GCP) and common Clinical Research SOPs
Preferably one or more years experience as a CRA in the pharmaceutical industry or CRO
Interpersonal, organizational and time management skills
Knowledge of Medical Terminology
Ability to operate in a multi-cultural atmosphere, within an international study team
Fluent in spoken and written English
Good verbal and communicational skills
Driving License
Ability to travel (inter)nationally
Ability to handle multiple priorities and timelines, attention to detail.