Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds

Job Details

CRA Oncology

Company: Chiltern
Location: Office Based Leiden, Or Home Based Netherlands
Reference: CRA - NL
Closing Date: 26 Feb 18
Type: Full Time
Salary (£): On Application

Job Summary:

Chiltern is looking to recruit CRA for our Oncology department to be home based or office based in Leiden. Full time, fixed term contract.


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 4,300 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 for our Oncology department to be home based or office based in Leiden. Full time, fixed term contract.




• 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

• 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

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


For more information about Chiltern International, please visit our web site at


Successful candidates will have the opportunity to be part of a growing company with a strong brand and professional employees that care about the work they are involved in. Chiltern is constantly working to develop training capacity, therapeutic expertise, new technologies and processes to be one of the leading CROs globally.


Working for Chiltern will offer an excellent opportunity to raise your profile and develop your career whilst giving you the flexibility to enjoy a good work life balance.


Please note that if your experience does not mirror that of our requirements for this role you may not receive a response

Apply for this job: CRA Oncology

Contact Information:

Address:  Netherlands
Schipholweg 111, 2316 XC Leiden, Netherlands

Tel:  +31 71 711 2500
Website:  Visit Our Web Site

Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.