Oncology CRA
- Company
- RBW Consulting
- Location
- Belgium
- Salary
- Salary: On application
- Posted
- 21 Jan 2021
- Closes
- 20 Feb 2021
- Ref
- HJ-RK-CRA-BEU-210121
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Responsibilities:
- Provide ongoing updates and support to project management
- Demonstrate a commitment to quality in all aspects of monitoring and clinical research
- Monitor Investigative Sites’ adherence to GCP, ICH guidelines and local regulations, and internal policies
- Supervise the conduct of clinical studies, ensure compliance with protocols, regulatory requirements, and good clinical practice
- Review, maintain and reconcile Trial Master Files against Investigator Site Files
- Provide county-specific expertise to ensure operational compliance with local regulations
- Work effectively with other departments and levels within the organisation
Requirements:
- Minimum of 1 year experience as CRA
- Scientific degree/education preferred
- Background in medical and/or scientific knowledge preferred
- Knowledge of regulatory environment and guidelines (ICH, GCP, CFR, EU CT directive and local laws)
- Ability to travel extensively, including overnight stays
- Fluent in French, Dutch, and English
- Ability to work effectively across cultures
- Ability to drive a car and have a valid driver’s license – as required
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: +44 1273 952187.
Salary: On application