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Clinical Research Specialist

📁
Clinical
📅
19000JBO Requisition #
Careers that Change Lives
At our Bakken Research Center in Maastricht, about 400 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.

A Day in the Life
We offer you a position in which you, as a team member of the Cardiac Rhythm Management clinical group in CRHF:
  • (Assist in) Developing, designing and executing clinical studies;
  • Ensures compliance with regulatory directives / guidelines and the Clinical Investigation Plan;
  • (Assist in) Planning and coordinating project activities to ensure timely completion of the investigation;
  • Develops and maintains a high level of medical, technical and clinical expertise through relevant literature, scientific meetings, and interaction with various inside/outside experts;
  • Reports on progress and results of clinical investigations;
  • Interprets, evaluates and analyzes clinical data, provides interim / final reports; coordinates/contributes to publications;
  • Plans and coordinates clinical study team / hospital staff training and (investigator) meetings;
  • Collaborates closely with key opinion leaders;
  • Partners with cross-functional project teams, e.g. R&D, Regulatory Affairs, Marketing and Sales;
  • Willing to travel.
Your profile
  • Masters or PhD degree in Life Sciences
  • 1-2 years’ experience supporting clinical/academic studies or similar
  • Experience and or affinity with project management
  • 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 site management, and local regulations. This means you are familiar with clinical research study design, GCP’s and regulatory compliance guidelines for clinical trials. Knowledge of ISO14155 is a plus, as well as experience with pivotal studies.
Besides the ability to manage multiple tasks you dispose of good problem-solving skills and a high attention to detail and accuracy.. Quality focus is a must. 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.

We Offer

In our 5th Tenet of our Mission we recognize the personal worth of employees by providing an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success. 
Also a competitive package is of course part of that. We offer a competitive salary and benefits package to all our employees:

·         28 holidays;

·         Possibility to purchase 8 extra vacation days;

·         Flexible working environment;

·         Annual Incentive Plan % depending on company results;

·         Pension scheme and group discount on healthcare insurances

·         Tax advantages on commuting, fitness plan, bicycle plan;

·         Training possibilities via Cornerstone/Harvard Manage Monitor/GetAbstract

·         Employee Assistance Program and Recognize! (our global recognition program)

·         Private Lease possibilities

 

Your Answer

Is this the position you were waiting for? Then please apply directly via the apply button! 


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