Search the 25 jobs at Care Access

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.

The QMS Coordinator will manage and improve the Quality Management System (QMS), ensure compliance with regulatory standards, oversee document control, facilitate staff training, and compile performance reports. The role involves technical support and workflow processes for an effective QMS.

The Study Start-Up Manager facilitates the start-up activities for clinical trials, including site evaluation and activation. This role involves leading cross-functional teams, managing regulatory submissions, and ensuring successful project timelines while communicating with stakeholders and supporting site staff.

The Operational Compliance Specialist will lead operational quality compliance initiatives, conduct compliance checks on clinical trial documents, support quality issue management, and ensure adherence to GCP regulations. This role requires maintaining relationships, providing training, and supporting process improvements to enhance operational quality and efficiency.

The Sub-Investigator will support clinical trial activities, ensuring compliance with study protocols, managing subject visits, reviewing study data, and performing assessments while collaborating closely with the Principal Investigator.

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.

The Sub-Investigator II will manage clinical research studies, ensuring compliance with protocols and regulations, performing physical exams, administering investigational products, and monitoring patient reactions. This role includes regional travel and telemedicine responsibilities, supporting clinical trials across the USA.

The Principal Investigator oversees clinical trials, ensuring compliance with regulations and protocols, supervising study teams, and maintaining participant safety. Responsibilities include training staff, evaluating study progress, and engaging with study monitors, all performed remotely with minimal travel.

The Site Manager oversees complex clinical trial protocols at Care Access Research sites, supporting sponsors and CROs while mentoring CRCs. Responsibilities include site support, patient coordination, documentation, and ensuring compliance with regulatory guidelines and standards. They engage in continuous learning in their therapeutic area and maintain effective communication with stakeholders.

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 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.

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.