This job is currently Archived,
Posted on : 17 January 2017
With the growth of our global Clinical Operations department we are looking for experienced Clinical Research Associates who will be involved in feasibility studies, setting up, monitoring and on-site quality control of multi-center international clinical trials in novel pharmaceuticals. Clinical Research Associate Office-based in Prague, Czech Republic Requirements University degree in Life Sciences, pharmacy, MD or RN Prior CRA experience with full scope of monitoring responsibilities; independent monitoring experience in the Czech Republic Hands-on knowledge of ICH GCP Good English skills Proficiency in standard MS Office applications Desire and ability to travel Excellent communication, planning and organizational skills Responsibilities Setup, coordination, monitoring and general administration of international clinical studies of novel medicinal products Conduct and reporting of all types of monitoring visits to clinical sites Communication with clinical investigators, vendors, and support services in regards to study progress Maintenance of appropriate documentation regarding clinical site management Participation in feasibility research Quality control, preparation for and attendance at company s audits Training of investigators and clinical trial team members We offer Excellent working conditions in our office in Prague Friendly team of clinical research professionals worldwide Competitive salary and benefits package Personal and professional growth; access to training opportunities To apply, E-mail your CV and application letter at firstname.lastname@example.org.
CZECH REPUBLIC PRAGUE
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