The IT System Administrator will support daily IT operations, manage remote workstations, implement IT policies, and ensure compliance with security practices.

The Content Designer creates engaging patient-friendly content for clinical trials, collaborating with teams to optimize content across various platforms and adhere to compliance standards.

Seeking Counsel for Privacy and Innovation to advise on global data privacy, support clinical trial operations, and manage compliance matters.

The Source Document Specialist is responsible for creating, maintaining, and controlling source documents for clinical trials ensuring compliance with guidelines. Duties include document design, version control, and communication with site staff.

Manage community engagement to enhance participation in clinical trials, focusing on outreach to healthcare providers and local organizations.

The Community Engagement Partner will establish relationships with local organizations, plan community events, and manage outreach initiatives to support health research and engagement.

The Manager of Central Study Coordinators oversees a team to ensure high performance and deliver study results while collaborating with sponsors and leadership.

The Region Manager oversees site operations, personnel management, and study conduct, ensuring quality and compliance while fostering team engagement.

The Site Support Solutions Manager for LATAM oversees team management, client relations, and operational effectiveness in clinical research, ensuring exceptional performance and study results.

The Manager of Digital Strategy and Performance leads digital marketing campaigns to enhance patient engagement, manages a team, and analyzes performance data for optimizations.

The Growth Marketing Manager enhances digital marketing through SEO strategies, technical website management, and data-driven growth analysis to optimize user engagement and conversion rates.

The Logistics Manager oversees logistics operations, leads teams, ensures compliance, manages site setup, and drives process improvements for clinical trials.

The CRC with Fibroscan certification performs non-invasive liver elastography procedures, works with clinical teams, and ensures compliance with study protocols.

The Provider Partnerships Representative will build and maintain physician networks for clinical studies, ensure high-quality customer service, and drive business growth through strategic partnerships.

The Principal Investigator manages clinical trial studies, ensuring protocol compliance, team training, and patient safety, while liaising with sponsors.

The Technical Project Manager II will manage technology solutions, prioritize project backlogs, lead vendor communications, and support users in clinical trials at Care Access.

The Referral Marketing Manager will enhance the Care for Friends Program through strategic planning, data-driven campaigns, and collaboration with internal teams to improve patient engagement and referral success.

Responsible for developing global budgets for clinical studies, ensuring competitive pricing, overseeing rate cards, and managing a team. Collaborates with business development for proposals and leads contracts negotiations.

As the Senior Manager of Global Study Budgets, you will develop and manage study-specific budgets, collaborate across departments, and mentor a team while ensuring compliance with contracts and financial strategy.

The Fibroscan Technologist performs non-invasive liver elastography procedures, ensuring high-quality imaging while following study protocols and maintaining patient care standards.