Search the 18 jobs at Care Access

The Senior Communications Strategist is responsible for developing and delivering marketing communications for patient engagement in clinical trials. This role includes crafting campaign messaging, collaborating with creative teams, and analyzing campaign effectiveness to meet recruitment goals.

The Manager of Central Study Coordinators is responsible for hiring, developing, and managing a team of Central Study Coordinators to ensure a high level of performance and deliver exceptional customer experience. Key duties include setting goals, reviewing performance metrics, facilitating team meetings, and collaborating with sponsor and leadership teams to achieve study results.

The IT System Administrator at Care Access will implement, configure, and maintain IT assets, supporting daily operations including account management and device administration. The role involves developing IT policies for a remote workforce, ensuring compliance with regulations, and providing tier-1 support. The ideal candidate will have extensive experience in IT administration and a strong understanding of cloud services and security practices.

The NetSuite Administrator is responsible for configuring, maintaining, and managing the NetSuite ERP system. Duties include gathering and analyzing business requirements, implementing solutions, user support, custom scripting, and managing integrations. They will also lead projects related to system upgrades and performance improvements while ensuring data integrity and providing analytics for decision-making.

As a Customer Experience Representative, you will manage incoming calls, assist participants with inquiries related to clinical trials, accurately document interactions, and collaborate with team members to enhance participant experience.

The Region Manager is responsible for managing clinical trial sites, focusing on personnel management, site profitability, and the conduct of studies while promoting a positive team environment and ensuring compliance with protocols. Duties include staff meetings, performance evaluation, onboarding new employees, and tackling operational issues effectively.

The Principal Investigator oversees clinical trials, ensuring compliance with industry regulations and the proper training of research staff. Responsibilities include reviewing study protocols, maintaining documentation, assessing patient safety, and providing oversight remotely for study sites. They must engage with the sponsor and manage all aspects of the trial's conduct to ensure the highest quality of care.

The Fibroscan Technologist performs non-invasive liver elastography procedures to assess liver health, working with patients and healthcare teams to ensure high-quality imaging. Responsibilities include executing study protocols, adhering to safety and quality standards, and maintaining patient confidentiality. The role requires effective communication and the ability to manage multiple tasks in a fast-paced environment.

The Business Development Director will drive growth by identifying sales opportunities, managing relationships with pharmaceutical, biotech, and medical device trial sponsors and CROs. Responsibilities include establishing customer relationships, educating them about Care Access capabilities, managing the sales cycle, and collaborating with other departments to support business growth, all while maintaining high ethical standards.

The Site Manager will oversee complex clinical trial protocols and therapeutic areas, support sponsors and CROs, mentor CRCs, and ensure adherence to regulations. Responsibilities include patient coordination, documentation, and effective relationship management with participants and stakeholders.

The Business Development Director will drive business growth at Care Access by identifying sales opportunities, establishing customer relationships, managing the sales cycle, and developing strategic partnerships. The role involves collaborating with various departments to ensure business development success and maintaining high ethical standards.

The Sub-Investigator will oversee clinical study protocols, ensuring compliance with regulatory standards and managing study subjects' medical issues during visits. Responsibilities include reviewing documentation, reporting adverse events, and conducting physical examinations. This role involves regional travel and telemedicine work.

As a Senior Study Start-Up Manager, you will facilitate the start-up activities necessary for selecting and activating studies at sites. Your responsibilities include leading global study start-up processes, managing client portfolios, reviewing study information, tracking timelines, communicating with stakeholders, and mentoring team members. You will work to optimize start-up processes and ensure successful site evaluations and activations.

The Senior Data Engineer will design and implement a scalable data platform, develop data pipelines, conduct data migration, and ensure data governance. Responsibilities also include enhancing data system performance, mentoring junior engineers, and supporting CI/CD practices in data engineering workflows.

As a Data Engineer, you will maintain and optimize the data architecture by designing and implementing data platforms and pipelines, supporting migrations, troubleshooting issues, and ensuring compliance with regulations. You will also address stakeholder requirements and provide training support to staff members.

Implement, configure, maintain, and support IT assets within the company. Support technology operations and implement necessary IT assets, configurations, procedures, and systems. Responsible for daily IT operations, network administration, software management, and device administration. Develop scalable and practical policies configurations for workstations and mobile devices. Manage remote workstations and cloud solutions. Stay up to date with security software and best practices. Train and direct system users on information systems usage. Document processes, procedures, and activities related to IT systems. Collaborate with cross-functional stakeholders to plan and implement solutions.

The Senior Director of Contracting oversees the contracting ecosystem at Care Access, leading the contracting team and collaborating with various departments to ensure compliance. Responsibilities include negotiating critical agreements, implementing improvements to contracting processes, and setting KPIs to enhance efficiency and effectiveness in contracts management.

The Project Lead manages client projects within the Clinical Delivery department, ensuring project success through effective communication and coordination. Responsibilities include developing project plans, tracking client satisfaction, managing budgets, and optimizing project outcomes based on clinical research protocols.