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The Customer Experience Representative will manage incoming calls, provide participant support related to clinical trials, route calls to appropriate departments, document interactions in systems, and collaborate with team members to enhance participant experience.
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The Technical Project Manager II at Care Access will manage technology and process solutions, particularly focusing on laboratory information management systems. Responsibilities include project planning, stakeholder management, backlog prioritization, and user support, requiring strong analytical skills and a solution-driven mindset.
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The Referral Marketing Manager will enhance the Care for Friends Program by developing strategic roadmaps, analyzing program performance, creating engagement materials, and executing targeted marketing campaigns. This role requires collaboration across teams, oversight of communication channels, and management of a Program Engagement Coordinator.
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The Senior Manager, Global Study Budgets will develop and manage competitive study budgets, create country-specific rate cards, oversee financial planning, and lead a team to support the organization's global portfolio. The role involves collaboration with various teams to ensure budgets align with business goals and contractual terms, as well as providing insights to senior leadership.
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The Senior Manager, Global Study Budgets is responsible for developing and managing study-specific budgets, ensuring compliance with contractual terms, collaborating with various teams to create competitive budgets, and overseeing the maintenance and updating of rate cards while leading a team responsible for financial analysis and budget creation.
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The Fibroscan Technologist is responsible for performing non-invasive liver elastography procedures. This role includes patient interaction, using specialized equipment to assess liver health, ensuring compliance with study protocols, and maintaining high-quality imaging and data accuracy in a clinical environment.
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The Provider Partnerships Manager at Care Access is responsible for establishing and maintaining a network of physicians to support clinical research studies. This role requires recruiting physicians, expanding the physician database, ensuring quality service, attending marketing events, and conducting meetings to drive study delivery.
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The Operational Compliance Associate is responsible for overseeing operational compliance at the research site level, ensuring data accuracy and quality for clinical trial projects, developing dashboard metrics, managing quality issues, and ensuring compliance with regulatory and sponsor requirements.
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The Operational Compliance Associate oversees the operational quality and compliance framework at the research site level, focusing on data accuracy, developing metrics, ensuring regulatory compliance, and implementing best practices to enhance efficiency and quality in clinical research.
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The Operational Compliance Associate is responsible for overseeing operational compliance at designated research sites, ensuring data accuracy, maintaining quality metrics, and collaborating with the Operational Compliance Team to address quality issues in clinical trials.
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The Global Privacy Associate will support the Global Privacy Program Manager with operational and strategic development of data protection compliance processes. Responsibilities include implementing global privacy requirements, assisting in compliance with regulations like HIPAA and GDPR, managing data privacy requests, and collaborating with various departments to support audits and assessments.
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The Program Engagement Coordinator will support the Care for Friends Ambassador Program by managing communications, responding to inquiries, and ensuring high-quality customer service to participants. They will maintain accurate records, assist with problem-solving, and identify process improvements while collaborating with internal teams. This role requires strong communication and organizational skills in a remote environment.
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The Digital Community Manager will build and manage digital community efforts, establish partnerships, and expand the organization's digital presence, while tracking engagement metrics and collaborating with marketing teams.
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The Sub-Investigator supports clinical research studies through travel and telemedicine, overseeing study protocols, administering investigational products, performing physical exams, and ensuring compliance with regulations. They collaborate with the Principal Investigator to monitor patient safety and document study visits, and provide ongoing assessments of subjects, including managing adverse events.
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As a Senior Data Test Engineer, you will ensure data integrity and compliance with standards for healthcare data. Your responsibilities include developing data quality strategies, executing data quality assurance tasks, leading stakeholder engagement, and leveraging Azure services and SQL for data quality management.
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The Data Engineer will build and maintain data architecture, including implementing pipelines and optimizing data systems. Responsibilities include overseeing data storage solutions, ensuring compliance with regulations, monitoring system performance, and providing support to staff.
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The Site Manager oversees daily activities at the site, ensures enrollment goals are met, manages site personnel and studies, collaborates with investigators, handles financial aspects, maintains the site, and fosters a positive environment. Responsibilities also include training staff, conducting performance appraisals, and ensuring compliance with regulations and standards.
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The Executive Director of Operational Compliance will lead compliance frameworks, ensure quality standards, manage SOPs, oversee training programs, and drive operational efficiency. This role involves collaborating across departments and maintaining regulatory compliance in clinical trial practices.
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The IT System Administrator will support daily IT operations including account and network management, device administration, and software management. Responsibilities include implementing IT policies, maintaining cloud solutions, training users, and ensuring compliance with security practices and regulations.
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The Manager, Central Study Coordinator - Retention oversees a team of coordinators, ensuring performance and participant satisfaction. Responsibilities include team management, setting and achieving goals, training, performance analysis, problem-solving, and collaboration with leadership to optimize program outcomes. The manager also engages directly with tasks to remain connected to the team's work and is responsible for maintaining compliance with clinical research regulations.