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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.
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