Clinical Research Monitor

Clinical Research Monitor (CRA)
Office location – Maastricht
Duration – 12 months
Standard Hours Per Week - 16hrs
Responsibilities may include the following and other duties may be assigned.

• Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.
• Develops and maintains liaison with clinical investigators, Clinical Research organizations (CRO), affiliated hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug or medical devices approval.
• Responsible for reviewing adverse event cases with investigators, determining and monitoring time, budget, schedules, preparing study documents, and issuing status reports.
• May assist with design, development, and monitoring of clinical evaluation projects.
• Trains investigators and site personnel. Includes headquarter and field Clinical Research associates (CRA).
• Implements and prepares the clinical development strategy as outlined by the clinical teams.
• May contact and recommend qualified investigators to perform studies and initiate clinical trials.
• Ensures recruitment and retention of patients.

 
ADDITIONAL REQUIREMENTS:

• Open to travel and work in the Netherlands and Belgium.
• Required languages: English and Dutch; Would be an asset: German and French skills to support monitoring activities in Germany and French speaking part of Belgium.

For further details, please contact Rudo Urayayi on +44(0)1727 817 616 or email a copy of your CV to rurayayi@achieva.co.uk