Clinical Trial Assistant (CTA) (m/f) at Occlutech GmbH in , Germany Job Opportunity 2018

Clinical Trial Assistant (CTA) (m/f) Occlutech GmbH April 2018 , Anyone want to get to your pleasant working environment along with challenging. In a work place that is friendly and also open with the moments, we ensure that each one gets an equal chance to continue to develop themselves and their careers having Occlutech GmbH. Occlutech GmbH possesses a friendly working environment, companionship, and mutual assist. The leaders inside the Occlutech GmbH is also actively manual, support, and cherish every positive thought given its personnel. We believe that every staff requires a balanced life. Now this Occlutech GmbH is hiring Clinical Trial Assistant (CTA) (m/f) with , to get quality human resources. The following is the entire information if you are enthusiastic about a career with Occlutech GmbH .

Clinical Trial Assistant (CTA) (m/f) April 2018
Occlutech GmbH

Occlutech is one of the leaders in developing innovative products for the treatment of structural heart disease. The Company manufactures and markets medical devices in well over 50 markets around the world. Occlutech operates facilities in Germany, Turkey and Sweden. For additional information please visit our website at
Clinical Trial Assistant (CTA) (m/f)
LOCATION: Jena, Germany
REPORTS TO: Clinical Research Manager (CRM)
POSITION DESCRIPTION: The CTA will assist in the conduct of Clinical trial activities such as to support in submission process, to ensure appropriate documentation and to prepare relevant trial specific documents and communication with trial sites. This position is a part-time position (30 hours/week) for one year and located in Jena.
A young and motivated team will welcome you to meet together the challenges of clinical research. After an introduction period, you will have freedom for self-organization to fulfill your tasks. We also offer opportunities for further professional development.
PRINCIPAL RESPONSIBILITIES:You will be responsible for:
Support in Conduct of clinical studies and registries according to all applicable regu-lations, to commonly accepted practices, and to Occlutech’s internal guidelines.
Preparation and Maintain Sponsor File
Preparation of study-specific documents
Support Clinical Project Management in any study activities
Track record of Study Document
Prepare and documents Meetings
If required, assist in Study audits
Perform other related duties and responsibilities, on occasion, as assigned
Knowledge of regulatory clinical research framework, standards and guidelines
Excellent interpersonal and communication skills & team player
Fluent in English, verbally and in writing
Professional Experience in medical device industry and/or clinical research
Strong analytical and problem solving skills
Hands-on working style
Proven track record of working in a dynamic, international environment
Excellent skills in relevant Microsoft office software programs
Applicants must provide a CV & cover letter stating their interest in the position and their qualifications. References will be required. Please send your application (all documents together in one pdf file) to:
Occlutech GmbH
Frau Katrin Biedermann
Wildenbruchstraße 15
D-07745 Jena
[email protected]
Tel: 03641-508323

Task seekers expected to be able to continually be wary of any kind of dupery on behalf of Occlutech GmbH. Dialing recruitment procedure of new Occlutech GmbH April 2018 be performed only through a established email Occlutech GmbH. Send your own job application, although not openly back again a job as you desire. Many of us would appreciate almost any comments or tips so we could provide much better providers and provide facts article fuller work make it considerably more beneficial. We are always seeking often the best talent. I would like to show some gratitude to your visit about this internet site.

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