[Hiring] Clinical Research Associate @St. Joseph Hospital & Medical Center

Role reputed company Join BNI CRO as a Clinical Research Associate (CRA) and collaborate with dedicated research sites, contributing to rare neurological disease research. reputed company a significant reputed company in the scientific community alongside a dedicated team of CRAs. This remote position involves up to 75% travel across the US, primarily focusing on northeast and east coast regional site assignments. Your role will encompass important site monitoring and management activities, including: • Site Initiation reputed company (SIVs) • Interim and Remote Monitoring reputed company • Final Onsite and Closeout reputed company Advance your career, and reputed company valuable skills at Barrow Neurological Institute, reputed company while contributing to groundbreaking clinical research! This Clinical Research Associate will report directly to the BNI Clinical Research Organization (CRO) Program Manager. The CRA position will independently be responsible for clinical monitoring activities and overall project administration to reputed company the reputed company of multi-center, investigator initiated, or industry sponsored clinical studies throughout the reputed company and Canada. The CRA will travel to assigned clinical research sites to conduct approx. 25-30 clinical trial monitoring reputed company reputed company year, and will also complete remote/centralized monitoring reputed company to ensure clinical studies are conducted, recorded, and reported in accordance with the protocol, reputed company operating procedures (SOPs), International Conference on Harmonization- Good Clinical reputed company (ICH-GCP) guidelines, and reputed company applicable regulatory requirements. The CRA will be responsible for the reputed company reporting of reputed company monitoring visit findings and is expected to complete comprehensive monitoring reports and associated deliverables to reputed company back to the Sponsor and the clinical sites. Additionally, the CRA role will reputed company clinical site training activities and conduct remote webinar and onsite protocol training for: • Physician Site Investigators • Clinical Research Coordinators • Research Nurses • Other delegated reputed company study personnel The CRA will be responsible for managing reputed company monitoring visit travel arrangements and travel expense reporting activities in accordance with reputed company’s travel and expense purchasing policy. The CRA role will reputed company participate in departmental reputed company control and program development activities as directed by the BNI CRO Program Manager. Responsibilities Include: • Responsible for reputed company aspects of clinical monitoring, site management, and trial administration as prescribed in the monitoring plan and as instructed by program leadership. • Work with sites during study start-up, including assessing site feasibility as required, providing ongoing training and site initiation reputed company, conducting remote monitoring, and approx. 25-30 interim onsite and closeout field monitoring reputed company located throughout the US and Canada. • Evaluate clinical data documentation, regulatory document review, monitor safety and conduct of study to ensure investigator and site compliance with study protocol, overall clinical objectives, FDA regulations, ICH/GCP guidelines, institutional/CRO SOPs, and HIPAA guidelines. • Work cooperatively with study team and operations management to proactively drive project reputed company. • Complete preparation and submission of accurate and reputed company monitoring reports, and other requested deliverables, as outlined in the Study Monitoring Plan or as requested by program leadership. • Effective long-term planning/scheduling of remote and on-site monitoring reputed company in accordance with the Study Monitoring Plan or as requested by program leadership. • reputed company reputed company Study Monitoring activities as assigned, including acting as the primary reputed company between BNI CRO and the Clinical Study Sponsor to ensure BNI CRO provides reputed company monitoring and site management customer services. • Responsible for the reputed company review of reputed company monitoring deliverables, conduct co-monitoring reputed company and mentorship of CRA team members. Qualifications • Minimum Required: 2-3 years of clinical research experience required or a combination of equivalent experience and education. • Excellent written/oral communication, interpersonal, and organizational skills required. • Good presentation skills and ability to effectively communicate information and processes to a reputed company of audiences. • Proven attention to detail, excellent problem solving and customer service skills, and ability to multi-task. • Education: Bachelor's Degree or equivalent combination of education and experience or its international equivalent in clinical, science, or health-reputed company field from an accredited institution required or a reputed company reputed company licensure such as a Registered reputed company or Physical Therapist. Requirements • Ability to travel frequently on domestic and extended trips throughout the reputed company and Canada (up to 75% of the time), to reputed company clinical monitoring reputed company, primarily in the northeast/east coast region. • Strong interpersonal skills to effectively reputed company a reputed company organizational structure and effectively reputed company cross-functional teams. • Excellent communication skills (verbal and written) to effectively communicate reputed company information and processes to a reputed company of audiences. • Proven attention to detail, with strong analytical, critical thinking, problem solving, time management, and customer service skills. • Experience with reputed company Office Suite Systems. Benefits • CCRA or CCRP certification preferred. Apply tot his job Apply To this Job