Post Market Studies Manager Jobs
Clinical Studies Manager Jobs
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Post Market Quality Operations Manager
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At United States
Senior Post-Market Quality Engineer – Risk (Remote/Northridge, Ca)
By Medtronic
At , Northridge, 91325, Ca
Are you looking for an exciting opportunity to lead post-market studies and help shape the future of healthcare? We are looking for a Post Market Studies Manager to join our team and help us develop and execute post-market studies to ensure the safety and efficacy of our products. You will be responsible for managing the design, implementation, and analysis of post-market studies and will have the opportunity to collaborate with a diverse team of experts. If you are a strategic thinker with a passion for healthcare, this is the perfect job for you!
Overview The Post Market Studies Manager is responsible for the design, implementation, and analysis of post-market studies to assess the safety, efficacy, and performance of medical devices. This role requires a strong understanding of the medical device industry, regulatory requirements, and clinical research. The Post Market Studies Manager will work closely with internal and external stakeholders to ensure that post-market studies are conducted in accordance with applicable regulations and standards. Detailed Job Description The Post Market Studies Manager will be responsible for the design, implementation, and analysis of post-market studies to assess the safety, efficacy, and performance of medical devices. This role requires a strong understanding of the medical device industry, regulatory requirements, and clinical research. The Post Market Studies Manager will work closely with internal and external stakeholders to ensure that post-market studies are conducted in accordance with applicable regulations and standards.The Post Market Studies Manager will be responsible for:
• Developing and implementing post-market studies to assess the safety, efficacy, and performance of medical devices
• Designing and executing post-market studies in accordance with applicable regulations and standards
• Analyzing and interpreting data from post-market studies
• Developing and maintaining relationships with internal and external stakeholders
• Ensuring that post-market studies are conducted in a timely and cost-effective manner
• Preparing reports and presentations to communicate study results
Job Skills Required
• Knowledge of medical device industry and regulatory requirements
• Knowledge of clinical research and study design
• Ability to analyze and interpret data
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Strong organizational and project management skills
• Proficiency in Microsoft Office
Job Qualifications
• Bachelor’s degree in a related field
• 5+ years of experience in medical device industry
• 5+ years of experience in clinical research
• Experience in post-market studies
• Certification in Good Clinical Practice (GCP)
Job Knowledge
• Knowledge of medical device industry and regulatory requirements
• Knowledge of clinical research and study design
• Knowledge of post-market studies
• Knowledge of Good Clinical Practice (GCP)
Job Experience
• 5+ years of experience in medical device industry
• 5+ years of experience in clinical research
• Experience in post-market studies
Job Responsibilities
• Developing and implementing post-market studies
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