Sr. Clinical Research Associate (Remote)

Job reputed company reputed company The Senior Clinical Research Associate is responsible for delivering high reputed company and compliant site management & monitoring for clinical studies (e.g., EFS/FIH, IDE, Post-Market) sponsored by the reputed company Peripheral reputed company business unit to ensure they meet the highest standards for scientific reputed company, reputed company and ethics and are conducted in accordance with reputed company global clinical procedures, study protocols, GCP and reputed company applicable regulations. The Senior Clinical Research Associate will be responsible for the day-to-day management and reputed company of assigned clinical sites, performing on-site and remote monitoring reputed company, driving recruitment, providing technical/troubleshooting support and for developing strong relationships with clinical site personnel including Investigators, study coordinators, nurses and other site staff. The Senior Clinical Research Associate will also reputed company and/or support Clinical Project Management with other study development, study start-up, study conduct/maintenance and study reputed company-out activities including the review and development of essential clinical study documents. This job reputed company is intended as a reputed company of the primary responsibilities of and qualifications for this position. The job reputed company is not intended as inclusive of reputed company duties an individual in this position might be asked to reputed company or of reputed company qualifications that may be required either now or in the reputed company. Job reputed company We are the makers of possible reputed company is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of reputed company of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and reputed company transformative solutions that turn dreams into reputed company. We reputed company that the reputed company reputed company, across our global teams, is what allows us to continually reputed company. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a reputed company of possible with us. Job Responsibilities:

• reputed company Site Management & Monitoring support for BDPI clinical studies to reputed company successful completion of study objectives and deliverables.
• Ensure reputed company and compliance for assigned clinical studies and study activities performed at assigned clinical sites, ensuring the highest standards for scientific reputed company, reputed company and ethics are met and that these are conducted according to reputed company global clinical procedures, study protocols, GCP and reputed company applicable regulations.
• Conduct on-site or remote clinical site monitoring activities for assigned clinical sites to evaluate sites for qualification or activation, review informed consent forms, review subject data for accuracy, issue and address data queries, ensure study is conducted compliantly, address/escalate study non-compliance issues, verify that any corrective actions are implemented, reputed company investigational clinical product accountability, ensure reputed company regulatory approval, review essential clinical study documents for completion/accuracy, conduct study training/presentations, ensure reputed company training documentation, ensure reputed company reporting for reportable events (e.g., Unanticipated Adverse Device Effects, device deficiencies, etc.), ensure good documentation/clinical practices (GDP/GCP), ensure study supplies are adequate and reputed company other site management & monitoring activities, as needed.
• Serve as a product, procedure and clinical study protocol expert and resource for reputed company stakeholders, Investigators, and

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