Cedent Consulting Inc.
Cedent Consulting Inc. is a Dallas-based company that specializes in IT and clinical consulting services. The company focuses on providing expertise and counsel to clients by fostering joint teams to oversee projects from inception to implementation. With a global presence, Cedent delivers measurable results in IT service delivery, clinical trial management, and strategic planning, emphasizing business objectives over technical details.
Clinical Research Associate - Cardiovascular
September 30, 2024
Cedent Consulting Inc.
Cedent Consulting Inc. is a Dallas-based company that specializes in IT and clinical consulting services. The company focuses on providing expertise and counsel to clients by fostering joint teams to oversee projects from inception to implementation. With a global presence, Cedent delivers measurable results in IT service delivery, clinical trial management, and strategic planning, emphasizing business objectives over technical details.
📋 Description
• This is a remote position. • Position: Clinical Research Associate (CRA) Cardiovascular. • Location: Remote (applicant should be willing to travel as needed). • Job Overview: We are seeking a dedicated and detail-oriented Clinical Research Associate (CRA) with a strong background in cardiovascular studies. • The ideal candidate will play a crucial role in the management and monitoring of clinical trials, ensuring compliance with regulatory requirements, study protocols, and GCP guidelines. • Key Responsibilities: Study Monitoring: Conduct on-site and remote monitoring visits to assess study compliance, patient safety, and data integrity. • Site Management: Collaborate with site staff to facilitate the successful execution of clinical trials, including training and support for site personnel. • Data Review: Review and verify clinical data collected to ensure accuracy and adherence to protocols. • Regulatory Compliance: Ensure that all clinical activities comply with FDA regulations, ICH guidelines, and institutional policies. • Documentation: Maintain thorough documentation of monitoring visits, site communications, and any findings or issues. • Adverse Event Reporting: Oversee the identification and reporting of adverse events, ensuring timely and accurate documentation. • Study Coordination: Assist in the preparation and submission of regulatory documents, ethics committee submissions, and study materials. • Collaboration: Work closely with cross-functional teams, including project managers, data managers, and medical monitors, to support study objectives. • Training: Provide training and guidance to site staff on study protocols and procedures.
🎯 Requirements
• CRA certification (e.g., ACRP, SOCRA) is preferred.
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