Oncology CRA

Location Belgium
Discipline: Clinical Research
Job type: Permanent
Salary: £Salary: On application
Contact name: Roxanna Keshavarz

Contact email: Roxanna.Keshavarz@rbwconsulting.com
Contact phone: 01293584300
Job ref: 21229(i)
Published: 30 days ago
Expiry date: 15 April 2021

​This will be a home based role and single sponsor dedicated with a company car included.

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:

  • 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: roxanna.keshavarz@rbwconsulting.com / +44 1273 952187

Salary: On application