Oncology CRA

Location
Belgium
Salary
Salary: On application
Posted
21 Jan 2021
Closes
20 Feb 2021
Ref
HJ-RK-CRA-BEU-210121
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