📋 Role Overview & Responsibilities
Company Description VDyne is a start-up medical device company developing a catheter based technology for the treatment of valvular heart disease.
Role Description This is a full-time on-site role for a Clinical Project Manager at VDyne, Inc located in Maple Grove, MN. The Clinical Project Manager will be responsible for overseeing clinical research projects, ensuring compliance with regulatory requirements, managing project timelines and budgets, and coordinating with cross-functional teams. They will also collaborate with investigators, site staff, and external partners to ensure successful study execution and completion.
Qualifications Bachelor's degree in a relevant field such as Life Sciences, Nursing, or Pharmacy.Strong understanding of clinical research processes and regulations, including ICH-GCP guidelines, FDA regulations, and local country requirements.Experience working on multiple clinical studies simultaneously, including knowledge of study design, site selection, and feasibility assessments.Excellent project management skills, including the ability to develop and track project timelines, budgets, and resources.Strong communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams, investigators, and site personnel.Proficiency in using clinical trial management systems and electronic data capture systems.Certification in Clinical Research (e.g., CCRA, CCRP) is a plus.Knowledge of therapeutic areas related to the company's product portfolio is desirable.
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This position is located in Maple Grove, MN with potential relocation and sponsorship assistance depending on candidate qualifications.
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