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Clinical Trial Associate - Clinical Research Associate (NL/BE)

15.07.2019 REF: O190072 Leuven

Organization

The Clinical Company

Description of the Position

This position is aimed at graduates who have a keen interest in starting their career in clinical research. You will start as a Clinical Trial Assistant for a period of 6 to 12 months before growing into the position of an international Clinical Research Associate.

- The Clinical Trial Assistant provides the administrative support to the clinical research teams in the full spectrum of the research activities such as pre-clinical research, study start up, site management and site closure.
- The Clinical Trial Assistant assists in gather and the preparation of documents for clinical trial applications for the submission and approval from the competent authority and ethical committees.
- The Clinical Trial Assistant Is responsible for the correct filing and archiving of clinical trial documents, and the maintenance of study files.
- Provides support in meeting activities such as organizing and planning of meetings (e.g. investigator-, project-, team- meetings), and provide meeting minutes.

The Clinical Research Associate:
- is responsible for the set-up, initiating, conduct and closure of his/her investigational sites on assigned projects.
- performs and coordinates all aspects of the clinical monitoring and site management process of clinical trials in accordance with ICH-GCP, FDA guidelines, local regulations and Company Standard Operating Procedures.
- develops and maintain collaborative relationships with investigational sites and client company personnel.
- conducts site visits to assess protocol and regulatory compliance and manages required documentation to ensure patients are recruited within timelines and managed both safely and effectively in order to meet the study targets.
- develops and maintains knowledge of different therapeutic areas of science and medicine in order to facilitate study conduct, understand patient management and ensure adequate reporting.

Demands of the Position

• Degree in medicine, nursing, health care/life sciences or related fields.
• Knowledge of the ICH-GCP, local legislation and clinical trial related procedures.
• Excellent organization and management skills.
• Excellent communication skills.
• Fluent in at least Dutch and English + another EU language (f.e. French, Spanish, German,...)
• Motivated and eager to learn.
• Prepared to perform clinical monitoring on an international level.

Terms of Employment

Within The Clinical Company you will be part of a Benelux team of about 65 enthusiastic clinical professionals under the support of 3 dedicated Clinical Team Managers. We want our employees to be happy, motivated and secure in their job. We focus on training, coaching and career development and provide a long term contract and competitive benefit package. We offer the ultimate experience to join our internal team, working on projects for our several top (Bio) Pharmaceutical, Medical Devices and Biotech clients.
Interested in this challenge and want to apply directly?! Please use the apply button below. For more information, feel free to contact Nick Dufour at 0032 (0)475/87 02 36 or n.dufour@theclinicalcompany.com.

Nick for Belgium

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+32 475 87 02 36n.dufour@theclinicalcompany.com

Simone for the Netherlands

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+316 12996359simone.polman@theclinicalcompany.com

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