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Sr Clinical Research Specialist, Mounds View, MN, Atrial Fibrillation (AF) Solutions

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Clinical
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2000007S Requisition #
Thanks for your interest in the Sr Clinical Research Specialist, Mounds View, MN, Atrial Fibrillation (AF) Solutions position. Unfortunately this position has been closed but you can search our 1,354 open jobs by clicking here.
Must Have (Minimum Requirements):

To be considered for this role, the minimum requirements must be evident on your resume.

  • Bachelor’s degree required and minimum of 4 years of clinical research/medical writing experience within healthcare industry, or advanced degree with a minimum of 2 years clinical research/medical writing experience within healthcare industry

Nice to Have (Preferred Qualifications):

  • Master’s or PhD degree(s) in biomedical sciences or technical disciplines
  • Clinical research experience at Medtronic or within a medical device industry
  • Direct experience with medical and/or scientific writing within a medical device industry or related industry
  • Scientific knowledge in cardiovascular physiology and cardiac arrhythmias
  • Proficient knowledge of physiology and/or applicable disease states, AF therapies and technologies
  • Proficient knowledge of current regulatory agency guidance and regulations, including EU MDR and MEDDEV Rev 4
  • Proficient knowledge of medical terminology, clinical research study processes, basic statistical concepts, demonstrated ability to incorporate and adhere to regulatory standards
  • Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials.
  • Possess strong understanding of study design, metrics and medical writing 
  • Experience working on a Global study team
  • Proficiency in MS Office applications: Excel, PowerPoint and Word, Project (or similar scheduling software), project management techniques and tools; and web-based applications.
  • Experience in managing clinical trial data review.
  • Ability to incorporate and adhere to good clinical practices and regulatory standards.
  • Ability to manage multiple clinical research sites with proven results in study execution.
  • Ability to identify and implement solutions in addressing study issues.
  • Basic understanding of biostatistics and trial design.
  • Proficient knowledge of medical terminology.
  • Excellent project management and organization skills. 

About Medtronic

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services 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 want to 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. 

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

 

About 5-10% of time will be spent in the field and this travel may include international travel.


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