Alcanza Clinical Research
Healthcare Insurance • Biotechnology • Science
Alcanza Clinical Research is a company dedicated to advancing clinical research through inclusive and impactful methodologies. They facilitate the participation of diverse populations in clinical trials by lowering barriers and ensuring high-quality research practices. Alcanza collaborates with medical providers and community organizations to provide patients with access to cutting-edge treatment options and health education across various therapeutic areas, without requiring insurance. Participants can benefit by receiving healthcare access, emerging treatments, and compensation for their time. The company is committed to patient safety and data integrity, providing opportunities for individuals to contribute to healthcare advancements across many locations in the United States.
Clinical Research Systems Coordinator – Clinical Conductor Experience Required
2 hours ago
Alcanza Clinical Research
Healthcare Insurance • Biotechnology • Science
Alcanza Clinical Research is a company dedicated to advancing clinical research through inclusive and impactful methodologies. They facilitate the participation of diverse populations in clinical trials by lowering barriers and ensuring high-quality research practices. Alcanza collaborates with medical providers and community organizations to provide patients with access to cutting-edge treatment options and health education across various therapeutic areas, without requiring insurance. Participants can benefit by receiving healthcare access, emerging treatments, and compensation for their time. The company is committed to patient safety and data integrity, providing opportunities for individuals to contribute to healthcare advancements across many locations in the United States.
📋 Description
• 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 access permissions, study parameters, and data fields. • Collaborate with IT professionals to ensure the proper 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 milestone 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 security measures such as MFA and SSO. • Stay abreast of updates to SaaS platforms, disseminate patch notes to relevant stakeholders, and manage version control and release processes. • Ensuring ongoing validation and providing documentation to sponsors as required. • Lead system and data migration processes, ensuring data integrity and minimizing operational disruption. • Maintain a comprehensive inventory of all active systems and manage their lifecycles in accordance with the IT Governance committee’s directives. • Provide application-level support to users, including oversight 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 continuous support and training for users. • Coordinate training sessions and provide resources to enhance user proficiency and efficiency. • Other related duties as assigned.
🎯 Requirements
• An Associate’s degree and 1+ years’ related experience with clinical research systems OR an equivalent combination of education and experience is required. • Strong proficiency with computer applications such as Microsoft applications, email, web applications, as well as clinical research systems applications. • Strong organizational skills and attention to detail. • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, management, and external customers. • Well-developed written and verbal communication skills. • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities. • Must be professional, respectful of others, self-motivated, and have a strong work ethic. • Must possess a high degree of integrity and dependability. • Ability to work under minimal supervision, identify problems and implement solutions. • Ability to handle highly sensitive information in a confidential and professional 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, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
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