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Job Details

Senior Clinical Research Associate

Company: Amoria Bond
Location: Netherlands
Reference: J69438
Closing Date: 05 Dec 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Senior Clinical Research Associate – South Holland (12 Months-Perm) Clinical Research Associate CRA Project management, Senior Clinical Research, Clinical Research Associate, Pharmaceutical, Biotech, Permanent, Netherlands, Clinical research, Senior CRA My client is a clinical research organisation, committed to improving access to healthcare and supporting the people they serve throughout the continuum of care. ...

Requirements:

Senior Clinical Research Associate – South Holland (12 Months-Perm)

Clinical Research Associate

CRA Project management, Senior Clinical Research, Clinical Research Associate, Pharmaceutical, Biotech, Permanent, Netherlands, Clinical research, Senior CRA

My client is a clinical research organisation, committed to improving access to healthcare and supporting the people they serve throughout the continuum of care. They are currently expanding their clinical operations team to welcome a senior Clinical Research Associate (CRA) to work on several studies at their offices in Zuid Holland. This is a 12 month contract with the possibility of a permanent offer thereafter.

The successful Senior Clinical Research Associate will be working on a number of studies (pharma, patient treatment, cardiovascular, post marketing etc.). Having risk based monitoring experience is essential, and they require someone with broad experience as a CRA. The role is office based, with a full week consisting of 36 hours.


The successful Clinical Research Associates will have
• Degree level education in Health Sciences or a relevant discipline and/or considerable knowledge working as a Clinical Research Associate
• Risk based monitoring experience is essential, with experience using clinical data softwares (SDV etc)
• Previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) for research sites in compliance with the approved protocol
• Experience in clinical study protocol development and ethical submissions
• Excellent communication skills for ongoing communication with the medical site staff (coordinators, clinical researchers and their site staff)
• Advanced proficiency in English & Dutch, both verbal and written.

The Role
• Monitor clinical trials to ensure absolute adherence to good clinical practice in accordance with ICH-GCP standards.
• Site management to ensure adequate adherence to protocol, source data verification and assess CRF entries
• Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
• Liaise with the Medical Monitor, Principle Investigator, Clinical Operations staff and sponsor representatives as required
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements

Get in touch

If you think you meet the criteria for this role, please apply to this post or forward your CV to me directly at Rohaan.khancv@amoriabond.com

Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.

Apply for this job: Senior Clinical Research Associate

Contact Information:

Address:  Head Office
Keizersgracht 270, 1016 EV Amsterdam, Nederland.

Netherlands
Tel:  +31 (0) 20 80 80 888
Website:  Visit Our Web Site

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