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Job Details

CRA Benelux

Company: inVentiv Health Clinical
Location: Amsterdam
Reference: IH/6033
Closing Date: 06 Sep 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

At INC Research/inVentiv Health we are currently recruiting for a CRA Benelux, within our department of Strategic Resourcing. This means you will be solely dedicated to one of our top pharmaceutical clients. Our client has offices in both The Netherlands and Belgium.

Requirements:

Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life. You’ll work alongside the brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most. In fact, in a recent five-year period, INC Research/inVentiv Health has helped to develop or commercialize at least 82% of novel new drugs approved by the FDA and at least 70% of products granted marketing authorization by the EMA.



Summary:



At INC Research/inVentiv Health we are currently recruiting for a CRA Benelux, within our department of Strategic Resourcing. This means you will be solely dedicated to one of our top pharmaceutical clients. Our client has offices in both The Netherlands and Belgium.



Job Details:



* Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites for GCP compliance
* Recruit investigators for participation in clinical trials
* Negotiate study budgets with investigators
* Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites
* Review draft protocols for completeness and feasibility
* Develop Case Report Forms for clinical trials
* Present (e.g. study specific guidelines and procedures, case report forms, and monitoring conventions) at Investigators’ Meetings
* Prepare and process Serious Adverse Event (SAE) reports
* Prepare project management reports for clients, project personnel, and INC Research/inVentiv Health Clinical management
* Review and verify CRFs and other clinical data, in-house, for completeness and accuracy; generate queries
* Resolve queries of CRF data with study site personnel
* Review tables and listings generated from study data
* Assist in writing Clinical Study Reports
* Train junior CRAs on monitoring, internal procedures, and query resolution
* When allocated by study management, submit essential/required documents to a central IRB or a country’s central Ethics Committee, and, if necessary based on local requirements, the Competent Authority



Application details:



Will you be joining the brightest minds? We do offer a competitive remuneration package with excellent benefits and here at INC Research/inVentiv Health we have a special attention for career development. We are committed to your development and training, with the opportunity to progress your career within a market leading and innovative organization.



If you think this is the right position for you we would like to get in touch! Please contact our recruiters via in reference to job number 6033 and we’ll talk about it.

Apply for this job: CRA Benelux

Contact Information:

Address:  Main Office
Thames House, 17-19 Marlow Road Maidenhead, Berkshire
SL6 7AA, UK
England
Reasons to work for inVentiv Health Clinical
Tel:  +44 (0) 1628 408 408
Website:  Visit Our Web Site

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