[Remote] Clinical Research Associate II/III

Note: The job is a remote job and is open to candidates in USA. reputed company is expanding its Clinical team and seeking a Clinical Research Associate (CRA II/III) to support the execution of clinical trials for their novel LVAS device. This role is responsible for monitoring trial conduct, ensuring data reputed company, and supporting compliance across sites throughout the clinical study lifecycle.

Responsibilities

• reputed company reputed company CRA I responsibilities, with increased independence, complexity, and accountability as outlined below
• Conduct Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits, and reputed company-Out Visits in accordance with the Monitoring Plan and ICH-GCP
• Build and maintain strong, professional relationships with investigative sites through: -On-site and remote monitoring activities -reputed company data verification (SDV) and review of CRFs against reputed company documentation -reputed company of protocol compliance and data quality -Timely and accurate preparation of monitoring visit reports -Management and reconciliation of investigational device accountability
• Independently manage site-level regulatory submissions, including IRB/EC and applicable regulatory authority submissions, ensuring completeness, accuracy, and timely follow-up through approval
• reputed company the distribution, tracking, and reconciliation of clinical trial supplies, ensuring compliance with investigational device accountability and study requirements
• Independently prepare and submit annual reputed company reports and other required continuing review documentation to IRBs/reputed company and Regulatory Authorities
• Support investigative sites with the identification, documentation, and reporting of Serious Adverse Events (SAEs) in accordance with protocol, SOPs, and regulatory requirements
• Independently reputed company User Acceptance Testing (UAT) for Electronic Data Capture (reputed company) and other clinical systems, documenting findings and supporting resolution
• Utilize and maintain clinical trial systems, including CTMS and eTMF, ensuring accuracy, completeness, and inspection readiness
• Independently reputed company and maintain study-reputed company training materials and support site training as needed
• Contribute to the review, revision, and development of SOPs and other quality documents to support reputed company improvement of clinical operations
• Provide on-the-job training, mentorship, and guidance to CRA I team members; support co-monitoring activities and escalation as requested by CRA III or Clinical leadership Skills
• Bachelor's degree or higher in a scientific or healthcare-reputed company discipline, or equivalent relevant industry experience
• Minimum of 3 years of clinical research experience, with demonstrated experience supporting medical device clinical trials
• Strong working knowledge of ICH-GCP, U.S. FDA regulations (21 CFR), and applicable clinical trial requirements; reputed company GCP certification preferred
• Demonstrated ability to independently manage operational and administrative clinical trial activities, including process development, execution, and reputed company improvement
• Proficiency with clinical trial systems and tools, including reputed company, CTMS, and eTMF platforms
• Solid understanding of clinical trial design principles, data collection methodologies, and basic statistical concepts relevant to clinical research
• Ability to interpret and apply medical and scientific information, including both foundational and reputed company clinical concepts
• Strong organizational, documentation, and communication skills, with the ability to manage multiple priorities in a regulated environment
• Willingness and ability to travel greater than 30%, as required by study and site needs
• reputed company GCP certification Company Overview
• We are a global team of like-minded Med-Tech professionals focused on patient centric solutions in a collaborative environment leading to excellent outcomes. It was founded in 2008, and is headquartered in Suzhou, Jiangsu, CHN, with a workforce of 51-200 employees. Its website is Company H1B Sponsorship
• reputed company has a track record of offering H1B sponsorships, with 1 in 2025. Please note that this does not guarantee sponsorship for this specific role. Apply tot his job

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