Clinical Research Specialist

1 week geleden


Maastricht, Limburg, Nederland Medtronic Voltijd

Unlock Your Potential in Clinical Research
Medtronic is seeking a highly skilled Clinical Research Specialist to conduct clinical studies in compliance with regulatory standards and align with business needs. As a key member of our team, you will monitor progress and results of clinical investigations, prepare clinical trial budgets, and oversee operational aspects of clinical trials. Your expertise in Good Clinical Practice (GCP) and regulatory compliance guidelines will ensure seamless study execution.

A Day in the Life of a Clinical Research Specialist
Key responsibilities include designing, planning, and developing clinical evaluation research studies for new products, preparing and authoring protocols and patient record forms, and conducting registered and non-registered clinical studies. You will also serve as a liaison between program management and planning, study team, and leadership, collaborating with a cross-functional team to drive project success.

Requirements and Qualifications
Our ideal candidate holds a Bachelor's degree in a relevant field with at least 2 years of clinical research experience or a Master's degree/PhD with no experience. Experience in clinical operations, developing clinical strategies, and study design is highly valued. Proficiency in GCP and regulatory compliance guidelines is essential.

What We Offer
Medtronic offers a competitive salary and benefits package, including flexible working environment, annual incentive plan, pension scheme, group discount on healthcare insurance, and training opportunities. Join a diverse team of innovators who bring their unique perspectives and experiences to drive healthcare forward.



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