The In-house CRA manages and supports clinical sites from approval through close-out, ensuring trial data integrity. Key duties include developing study documents, managing regulatory filings, and conducting remote data reviews.
Alira Health
17 Remote Job Openings at Alira Health
The In-house CRA manages and supports clinical sites from approval through close-out, ensuring trial data integrity. Key duties include developing study documents, managing regulatory filings, and conducting remote data reviews.
The Senior CRA is responsible for conducting site monitoring visits and providing leadership and oversight to the CRA team to ensure clinical trial quality and compliance. Key duties include reviewing monitoring reports, managing study budgets, and ensuring the integrity of CRF data through meticulous source document verification.
The intern will review, analyze, and upload a backlog of executed commercial contracts into the One Contracts system. Key tasks include ensuring document legibility and accurately logging metadata such as effective dates and obligations.
The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to regulatory standards. They also provide leadership and guidance to study sites while collaborating with cross-functional teams to manage trial execution and safety reporting.
The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and regulatory adherence. They also provide leadership and guidance to study sites while managing recruitment, training, and essential documentation.
The Senior Clinical Research Associate manages site monitoring responsibilities for clinical trials to ensure protocol compliance, quality, and adherence to timelines. They provide leadership and guidance to the CRA team while collaborating with cross-functional departments to resolve site-related issues.
The HR Operations Manager leads and evolves HR operational excellence across the United States and Canada, ensuring compliance and efficient service delivery. This role manages a diverse team, oversees daily HR operations, and partners with stakeholders to implement scalable process improvements.
The Senior Project Manager oversees clinical research studies to ensure compliance with protocols, budgets, and regulatory standards while serving as the primary contact for sponsors. They also supervise clinical team members and facilitate communication across various study functions to meet trial milestones.
The Sr CRA independently conducts site monitoring for clinical trials, providing oversight, leadership, and guidance to ensure compliance and quality across study execution. Key duties involve reviewing monitoring reports, ensuring timely site visits, coordinating issue resolution, and maintaining data integrity through meticulous source document review.
The Senior CRA independently conducts site monitoring for clinical trials, providing oversight, leadership, and guidance to ensure compliance and quality across study execution. Key duties include reviewing reports, ensuring site visit timeliness, coordinating issue resolution, and maintaining data integrity through meticulous source document review.
The Senior CRA independently conducts site monitoring for clinical trials, providing oversight, leadership, and guidance to ensure compliance and quality execution of study activities. Key duties include reviewing monitoring reports, ensuring timely site visits, assisting with site setup documentation, and managing study budgets for stand-alone projects.
The CRA performs site monitoring visits (selection, initiation, monitoring, and close-out) according to scope of work, SOPs, and regulatory requirements like GCP and ICH Guidelines. Key duties include driving subject recruitment, providing protocol training to sites, evaluating site practices, and ensuring proper informed consent and investigational product accountability.
The Senior Clinical Research Associate (Sr CRA) conducts site monitoring for clinical trials, ensuring compliance and quality while providing oversight and guidance to the CRA team. Responsibilities include managing study budgets, preparing monitoring reports, and maintaining communication with study sites.
The Senior Clinical Research Associate (Sr CRA) conducts site monitoring for clinical trials, ensuring compliance and quality. They provide oversight and guidance to the CRA team and coordinate with cross-functional departments to resolve clinical trial monitoring issues.
The Senior Clinical Research Associate (Sr CRA) conducts site monitoring responsibilities for clinical trials and provides oversight and guidance in the management and execution of these trials. They ensure compliance and quality by coordinating with various departments and addressing site-related issues.
Senior Consultants manage project execution and develop strategies to address client needs. They also oversee the creation of deliverables and ensure high-quality outcomes while fostering long-term client relationships.
