Company: Barrington James Clinical
Location: Spain, Belgium, France, Germany
Closing Date: 01 Jan 17
Salary (£): Competitive
Benefits: Great Benefits
Outstanding reviews - Leading company in Europe in Medical Devices working across niche Therapeutic areas - Perfect opportunity for someone looking to progress their career in the fastest growing therapeutic area on the market.
Exciting Opportunity - Home based/Office based positions in beautiful locations across France, Germany, Spain and Belgium - Outstanding reviews - Leading company in Europe in Medical Devices working across niche Therapeutic areas - Perfect opportunity for someone looking to progress their career in the fastest growing therapeutic area on the market.
Senior Clinical Research Associate
Planning, organizing, and monitoring clinical studies from initiation to close-out in the areas of Cardiac Rhythm Management (implantable pacemakers, defibrillators, electrodes) and Heart Valves in collaboration with national and international colleagues
Preparing and updating documentation, reports, handbooks, and guidelines
Providing clinical trial centres with assistance and support during clinical trials
Ensuring compliance with trial protocols and study-specific procedures
Monitoring and complying with quality management standards, internal SOPs, as well as budget and time allowances
Providing technical assistance to the product management team
Serving as a reliable contact person for the authorities in Germany and, if necessary, in Austria, Switzerland or in Eastern European countries
An apprenticeship as a medical technical assistant (MTA), pharmaceutical technical assistant (PTA), nurse, or holding a university degree with a background in medicine or the natural sciences
Three years of professional experience as a clinical research associate monitoring on sites, preferably in the area of medical devices
Knowledge of the respective laws and regulations
Good oral and written command of German and English; additional eastern European languages would be a plus
Knowledge of clinical software, e.g. Clinical Trial Management System, electronic Case Report Forms (eCRF)
Working knowledge of MS Office applications and computer literate
Willingness to travel on a frequent basis, also within Europe
Ability to work conscientiously, assertively, and independently, as well as excellent negotiation skills
What we offer:
We offer the assistance of an experienced team, as well as supporting you during your transition. Become a part of our expanding and internationally positioned company!
If you are interested in this challenging and varied position, then take the next step: Send us an English application stating your salary expectations and your earliest possible starting date.
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