Clinical Research Specialist

15 uur geleden


Maastricht, Limburg, Nederland Medtronic Voltijd
Careers that Change Lives

Are you ready for an exciting role as a Clinical Research Specialist, where you will be responsible for conducting clinical studies in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs? You will monitor progress and results of clinical investigations in preparation for device application and/or publications. You will be responsible for managing and meeting the objectives of a clinical study. Assumes project management responsibilities for selected studies and site management activities as needed.

A Day in the Life

Responsibilities may include the following and other duties may be assigned:

  • Assist in designing, planning, and developing clinical evaluation research studies for products that are under Clinical Investigation.
  • Prepares and authors protocols and patient record forms.
  • Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
  • Oversees and interprets results of clinical investigations in preparation for new device or consumer application.
  • Oversees and manages operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.
  • Serves as liaison between program management and planning, study team, and leadership.
  • Collaborates and partners with a cross-functional team which includes site managers, monitoring, safety, stats, and others
  • Assist in reviewing status of projects and budgets; manages schedules and prepares status reports.
Requirements

We are looking for a highly skilled and experienced Clinical Research Specialist to join our team. The ideal candidate will have:

  • Bachelor's degree required with a minimum of 2 years of clinical research experience (i.e., in the development and execution of clinical studies) or Master degree/Phd degree with 0 years of clinical research experience.
  • Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials.
  • Experience managing multiple clinical research sites with proven results in study execution.
  • Experience in clinical operations.
  • Experience developing clinical strategies and study design.
  • Experience in Peripheral Vascular therapies/product.
What We Offer

We offer a competitive salary and benefits package to all our employees:

  • Flexible working environment
  • Annual Incentive Plan % depending on company results
  • Pension scheme and group discount on healthcare insurance
  • Training possibilities via Cornerstone/Skills Lab
  • Employee Assistance Program and Recognize (our global recognition program)
Our Commitment

Our unwavering commitment to inclusion, diversity, and equity (ID&E) means zero barriers to opportunity within Medtronic and a culture where all employees belong, are respected, and feel valued for who they are and the life experiences they contribute. We know equity starts beyond our workplace, and we must play a role in addressing systemic inequities in our communities if we hope to have long-term sustainable impact. Anchored in our Mission, we continue to drive ID&E forward both to enhance the well-being of Medtronic employees and to accelerate innovation that brings our lifesaving technologies to more people in more places around the world.



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