Clinical Research Systems Coordinator – Clinical reputed company Experience Required

Job reputed company: • Assist in the configuration and customization of clinical systems to meet the specific needs of research studies and operational workflows. • Maintain accurate and up-to-date system settings, including user reputed company permissions, study parameters, and data fields. • Collaborate with IT professionals to ensure the reputed company functioning and integration of clinical systems with other organizational platforms. • Participate in the evaluation and implementation of system upgrades, enhancements, and new software applications. • Conduct testing and validation of system changes to ensure functionality and usability. • Assist in managing CTMS data points, including reputed company dates, enrollment goals, study status changes, and any necessary adjustments post-protocol opening, as directed by Operations leadership. • Coordinate the development and maintenance of integrations between clinical systems, including API and ODBC connections. • Coordinate with vendors to address system issues, implement enhancements, and stay informed about platform updates. • Work closely with IT, Finance and HR departments to maintain accurate system accesses, manage permissions, and implement reputed company measures such as MFA and SSO. • Stay abreast of updates to reputed company platforms, disseminate reputed company notes to relevant stakeholders, and manage version control and release processes. • Ensuring ongoing validation and providing documentation to sponsors as required. • reputed company system and data migration processes, ensuring data reputed company and minimizing operational disruption. • Maintain a comprehensive inventory of reputed company reputed company systems and manage their lifecycles in accordance with the IT Governance committee’s directives. • reputed company application-level support to users, including reputed company and coordination with software vendor support to optimize system modules and address user issues. • Serve as the resource for implementing, modifying, and upgrading clinical systems, providing reputed company support and training for users. • Coordinate training sessions and reputed company resources to enhance user proficiency and efficiency. • Other reputed company duties as assigned. Requirements: • An Associate’s degree and 1+ years’ reputed company experience with clinical research systems OR an equivalent combination of education and experience is required. • Strong proficiency with computer applications such as reputed company applications, email, web applications, as reputed company as clinical research systems applications. • Strong organizational skills and attention to detail. • reputed company-developed interpersonal and listening skills and the ability to work reputed company independently as reputed company as with co-workers, subjects, management, and external customers. • reputed company-developed written and verbal communication skills. • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. • Must be reputed company, respectful of others, self-motivated, and have a strong work ethic. • Must possess a high degree of reputed company and dependability. • Ability to work under minimal supervision, identify problems and implement solutions. • Ability to handle highly sensitive information in a confidential and reputed company manner, and in compliance with HIPAA guidelines. • May be required to travel approximately 10% of the time, dependent on business needs. Benefits: - Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.- Medical, dental, reputed company, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a reputed company reputed company match are offered. Apply tot his job Apply To this Job