Job Details

Company: Chiltern
Location: Heverlee
Reference: CRA - OCO
Closing Date: 19 May 18
Type: Full Time
Salary (£): On Application
Benefits: Excellent and competitive benefits

Job Summary:

Chiltern is looking to recruit CRA to be based in our office in Belgium.

Requirements:

Job Background

Chiltern is the leading, global mid-sized contract research organization. We listen to client needs to deliver customized clinical development solutions with a team of more than 4,200 working across 47 countries to provide comprehensive, yet flexible and responsive, services.  Our specialties include clinical development, Oncology, Devices and Diagnostics, Data, Analytics & Evaluation and Strategic Service Provision.

Chiltern is looking to recruit CRA to be based in our office in Belgium.

• Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.

• Assist with document submissions to local authorities

• To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required

• Ensure that all study related communication including e-mail is tracked, printed and filed as required

• To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA

• To liaise with all other appropriate departments within Chiltern International to ensure the smooth running of the study

• To assemble files and ensure documents for the trial master file accurately reflect the progress of the study

• A BSc or BA degree in a biomedical or related life science, or nursing qualification

• Previous CRA experience within clinical research of approximately 2 years

• Previous experience within Oncology is preferred

• Good clinical knowledge with an understanding of medical terminology

• An understanding of the basics of physiology and pharmacology

• Understanding of the principles of ICH GCP and regulatory requirements

• Experience using a clinical trial management system

• Preferable experience using a clinical trial management system (CPMS)

• Experience as a CRA on single site and/or multicentre trials

• Good oral and written communication, organizational skills and personal presentation

• The ability to communicate effectively in English, Dutch and French

• Good computer literacy with working knowledge of PCs, Windows and Microsoft Office    applications

Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.

On application

Permanent
Full Time

Email Kevin Thomas - kevin.thomas@chiltern.com
+33 01 41 05 73 53