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Clinical Trial Educator

12.08.2019 REF: O190076 Home-based

Organization

Global pharmaceutical company and is the partner of choice for innovative, patient-focused solutions

Description of the Position

We are currently looking for a Clinical Trial Educator (CTE), being located in Belgium. In this position, you will report to the CTE Team Lead and will be part of the global Clinical Operations team. The CTE is responsible for supporting sponsored clinical trials, through CRO oversight and interaction with investigational sites, within the assigned countries/territory. You will contribute to and support successful execution of clinical trial protocols and work as a cross-functional matrix team member.
Your tasks will include, but not be limited to, the following:

- Establish relationship with investigational sites and act as sponsor interface
Champion site specific recruitment plan and strategies, mitigate barriers to patient recruitment with stakeholders
- Interact with Vifor’s global Clinical Study Team, Vifor’s local medical staff, external Service Providers, and investigational site staff (including investigators and study coordinators) to assist with timely, efficient and high quality trial delivery throughout all stages of the study
- Support operational excellence of global clinical trials through CRO oversight activities, including but not limited to accompanied visits, monitoring report review, tracking of trial related metrics and input to respective project plans
- Ad-hoc member of the global Clinical Study Team
- Provide input into department SOPs and processes, and involvement into investigational site inspection and audit readiness activities

Demands of the Position

- Relevant University Degree (BSc) or Health Care Degree (e.g. RN) with a higher degree (e.g. PhD, MD, PharmD) being preferred
- Minimum of 5 years in the pharmaceutical industry, in a Senior CRA or Lead CRA role, including direct contact with study sites and KOLs
- Good understanding of the drug development process and clinical trial execution
- Familiar with clinical trial documentation and regulatory requirements
- Excellent knowledge of ICH GCP requirements
- Excellent user of Office Programs (Word, Excel, PowerPoint)
- Fluency in Dutch, English and French
- Willingness to travel (65% local and international travel required)

Terms of Employment

Contract direclty at the client's headcount
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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