Search the 35 jobs at Care Access

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.

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.

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.

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.

As an Instructional Designer, you will design and develop instructional materials, conduct needs analysis, and collaborate with subject matter experts. Your role includes creating engaging e-learning modules, storyboarding, media development, and ensuring LMS integration, while implementing assessment strategies for program effectiveness. Continuous improvement and staying updated with industry trends are essential.

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.

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.

The Digital Community Manager will engage communities through digital strategies, manage partnerships with organizations, and enhance the company's online presence. This involves creating meaningful connections and tracking engagement metrics.

The Manager of Loyalty Marketing will lead strategies to enhance patient loyalty and retention at Care Access. Responsibilities include managing a team, developing loyalty programs, analyzing campaign results, and ensuring regulatory compliance, all aimed at improving patient engagement.

The Central Study Coordinator manages clinical trial activities and provides virtual support to multiple research sites, ensuring quality data management and participant communication. Responsibilities include overseeing participant visits, facilitating informed consent, maintaining study documentation, and supporting site compliance, while also acting as a project manager for assigned studies.

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 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 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 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 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.

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 Training Coordinator at Care Access will manage training and development programs, assist with onboarding of new hires, identify training needs, and ensure compliance with training requirements. Responsibilities include supporting the training team, maintaining training materials, and executing the training matrix for operations staff.

The Sub-Investigator II at Care Access will oversee execution of study protocols, administer investigational products, and ensure site compliance. This role includes regional travel and telemedicine work, where the candidate will engage with study subjects and support clinical trial activities.

The Investigator Success Manager will drive partnership opportunities by onboarding new Investigators, conducting demos, and fostering relationships with physicians. Responsibilities include managing the onboarding process, recruiting clinicians, communicating the company's value proposition, and negotiating contracts. The role involves significant collaboration across departments and maintaining ongoing outreach with a network of Investigators.