Functietitel: (SENIOR) CLINICAL RESEARCH SPECIALIST

Functieomschrijving:
www.stepstone.be/vacatures----1402782-inline.html?cid=Partner_VDAB Covidien Job Posting Template Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We can accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future. Jobs.medtronic.com Medtronic Maastricht (SENIOR) CLINICAL RESEARCH SPECIALIST (m/w) - Job ID 255141 YOUR CAREER Medtronic offers you a professional, dynamic and high quality working environment, where personal development is stimulated and personal initiatives are encouraged. Your Individual Development Plan will challenge you to develop your personal skills and competencies, to build your career within our (global) organization. If you are interested in the role please contact our recruiter Natalia Latkowska under natalia.latkowska (at) medtronic.com and send us your CV and covering letter. OUR CHALLENGE At our Bakken Research Center in Maastricht, about 220 clinical researchers, scientists and technical engineers cooperate closely with medical specialists in and outside of Europe to develop new and improve existing therapies in Cardiac Rhythm Disease Management and Cardiovascular Surgery. Our broad range of clinical services, includes international project management, statistical advise, IT support and medical writing, which makes us Medtronic’s authority on clinical research outside of the US. OUR OFFER We offer you a position in which you will be responsible for designing, planning and implementing clinical studies in line with local regulatory requirements and overall business strategies. Your activities include protocol writing, overall project management, overseeing regulatory submissions, monitoring study progress and quality, and writing study reports. You will oversee CRO’s during the center start-up process, as well as during the course of the studies. The clinical data that you gather will support product approvals as well as scientific presentations and publications, in close cooperation with leading physicians in the field. YOUR PROFILE *Masters or PhD degree in Life Sciences *3-5 years' experience with direct support to clinical studies or similar *Strong networking skills *Significant detail orientation due to FDA submission *Able and willing to strictly follow procedures/SOP's, regulations and guidelines We are looking for a customer focused team player who is a clinical expert, specialized in clinical study management. This means you are familiar with clinical research study design, GCP's and regulatory compliance guidelines for clinical trials. Besides the ability to manage multiple tasks you dispose of good problem-solving skills and a high attention to detail and accuracy. You are used to take initiative and you demonstrate the ability to work effectively pro-active on cross-functional teams. You are a good communicator and fluent in English, both in writing and speaking. Frequent (inter)national travel is part of the job.

Werkgever Naam: Medtronic

Werkgever adres: Medtronic, , 6211 Maastricht, NEDERLAND

Vorm van contact: Medtronic

Job korte beschrijving: Natuurkundigen en astronomen

Land: Nederland

Regio: NEDERLAND

Contractduur: Vast

Contract type: Voltijds

Ervaring: Tussen 2 en 5 jaar

Bron van jobaanbieding:
VDAB, Openbare diensten voor arbeidsvoorziening, België

Hoe toe te passen: Overig - zie vrije tekst