Senior Clinical Research Specialist at Medtronic conducting pre- and post-market clinical trials internationally. Responsible for developing medical evidence for healthcare product safety and efficacy.
Responsibilities
Supervises, designs, plans, and develops clinical evaluation research studies.
Prepares and writes protocols and patient follow-up forms.
Conducts registered and unregistered clinical studies on products that meet a medical need and/or have commercial potential.
Supervises and interprets the results of clinical investigations for new applications for medical devices, drugs, or consumer products.
Manages and resolves the operational aspects of clinical trials in collaboration with project teams and in accordance with standard operating procedures (SOP), Good Clinical Practice (GCP), and applicable country regulations; prepares clinical trial budgets.
Responsible for clinical supply operations, site selection, and vendor management.
Requirements
Master’s degree in clinical sciences or a related field.
In-depth knowledge of the field, typically gained through higher education complemented by professional experience.
Practical experience in project management.
At least 4 years of experience in clinical research.
Benefits
Competitive salary and a flexible benefits package
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