Search the 22 jobs at Care Access

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 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.

The Sub-Investigator II supports clinical research studies, administering investigational products, performing physical examinations, and monitoring reactions. Responsibilities include overseeing study protocols, ensuring compliance with regulations, conducting virtual and in-person consultations, and maintaining proper documentation. The role requires travel and involves collaboration with a team to enhance clinical trial access.

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 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.

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 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 support clinical research studies, overseeing execution of study protocols, administering investigational products, monitoring reactions, and ensuring compliance with regulations. They will work both remotely and in-person with study subjects, perform physical examinations, and maintain communication with internal teams and investigators.

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.

The QMS Coordinator will manage and improve the Quality Management System (QMS), ensuring compliance with ISO and GCP standards. Responsibilities include maintaining QMS documentation, facilitating staff training, monitoring compliance timelines, performing system administration, and reporting on QMS performance.

The Operational Compliance Specialist leads operational quality compliance, conducts compliance checks on clinical trial documents, maintains quality support for regulatory compliance, and facilitates process improvement and CAPA management to enhance operational effectiveness and business success.

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 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.

The IT System Administrator will support daily IT operations by managing accounts, devices, and network systems, as well as designing and implementing necessary IT assets. They will ensure compliance with security standards while training users and documenting IT processes.