Search the 28 jobs at Care Access

The Senior Region Manager oversees clinical trial sites, ensuring site profitability and successful study conduct. Responsibilities include personnel management, staff training, performance evaluations, compliance with HR policies, and collaboration with site investigators. The role entails regular travel to various sites and fostering a positive team environment.

The Sub-Investigator II will support clinical research studies by overseeing study protocols, administering investigational products, conducting physical examinations, and ensuring compliance with regulatory standards. The role involves both regional travel and remote telemedicine work, interacting with study subjects, and maintaining high standards of patient care.

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.

The Senior Director of Contracting oversees Care Access's contracting team and strategy, ensuring efficient management and negotiation of agreements within healthcare and clinical research sectors. Responsibilities include leading team members, collaborating with internal stakeholders, drafting key contracts, and driving improvements in contracting practices.

The Sub-Investigator II is responsible for overseeing clinical research studies, ensuring compliance with protocols, administering investigational products, conducting physical examinations, monitoring patients, and managing study documentation. This role involves both regional travel and remote telemedicine work, requiring strong communication and organizational skills.

The Sub-Investigator II is responsible for supporting clinical research studies through administering investigational products, performing physical exams, ensuring compliance with study protocols, and managing adverse events. This role involves regional travel and remote tele-medicine work, requiring collaboration with site staff and excellent clinical skills.

The Source Document Specialist is responsible for creating, maintaining, and controlling source documents for clinical trials, ensuring accuracy, compliance with regulations, and managing version control while collaborating with site staff.

The Study Activation & Readiness Specialist ensures site readiness for clinical trials by supporting study compliance, managing essential documents, conducting training for site staff, and facilitating communication between stakeholders. They engage in problem-solving and coordination to streamline study activations and support operational improvements within the clinical research framework.

The CRC with Fibroscan certification performs non-invasive liver elastography procedures to assess liver health, collaborates with clinical teams to follow study protocols, ensures compliance with quality standards, and communicates effectively with patients and healthcare professionals.

The Pre-Screening Coordinator will facilitate oversight of lab result processes, ensuring labs are reported and escalated with appropriate medical supervision. Responsibilities include coordinating with staff, recording lab results accurately, escalating abnormal results, maintaining communication with laboratories, and performing quality checks of data.

As a Site Manager at Care Access, you will oversee complex protocols and therapeutic areas in clinical trials, support sponsors and CROs, manage site responsibilities, and ensure compliance with FDA regulations. You will also engage in patient coordination and documentation related to study management.

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 Principal Investigator oversees research studies to ensure compliance with regulations, manages study protocols, and trains research staff while engaging with sponsors and monitors to resolve issues. This role involves maintaining documentation, assessing participant responses, and ensuring safety in clinical trials.

The Provider Partnerships Representative at Care Access is tasked with building and maintaining relationships with specialist consultants and physicians, recruiting them for clinical research studies, and expanding the physician network. Responsibilities include managing inquiries, utilizing Salesforce for lead identification, and ensuring high-quality customer service while assisting in the overall business growth effort.

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 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 Instructional Designer at Care Access is responsible for designing and developing instructional materials that enhance employee learning. Key tasks include conducting needs analysis, designing curricula, storyboarding, developing multimedia content, and ensuring integration with the Learning Management System (LMS). The role also involves quality assurance, evaluating learning programs, and staying current with industry trends.

The Study Start-Up Manager at Care Access is responsible for leading the global study start-up process, facilitating site evaluations and activations, overseeing regulatory compliance, and providing guidance during the initial start-up phase. This role involves liaising with key stakeholders and ensuring seamless transitions of information to ensure efficient site activation for clinical trials.