As a Data Coordinator, you will manage clinical trial data integrity, support data collection and reporting, and assist in data analysis.

Oversee planning, execution, and completion of clinical trials while ensuring adherence to timelines, budgets, and regulations. Collaborate with teams and manage site relationships for successful outcomes.

The Senior Study Support Assistant provides administrative and operational support for clinical studies, facilitates communication among stakeholders, and trains junior staff.

The Senior Product Manager will lead end-to-end product delivery, collaborating across teams to align business needs with technology capabilities while ensuring continuous improvement and effective stakeholder engagement.

The Project Analyst II manages projects and tasks, working with teams and clients for successful execution within a clinical research environment.

Assist in coordinating and administering clinical trials, maintaining documentation, preparing study materials, and tracking clinical trial metrics.

As Proposals Manager, you will develop client proposals, collaborate with teams, analyze RFPs, manage proposal processes, and support team members.

As an IHCRA, you will support clinical trials by planning, conducting feasibility assessments, monitoring progress, and ensuring compliance with protocols.

The Site Specialist II will lead clinical trial initiation, manage regulatory submissions, ensure compliance, and improve study start-up processes.

The Site Specialist II oversees clinical trial site operations including start-up, maintenance, and contract management, ensuring compliance and effective communication across teams.

As a Site Specialist II, you will support site activation, vendor coordination, and ensure compliance in clinical research activities and documentation.

The Clinical Research Associate I will coordinate clinical trials, ensure compliance, manage study documentation, and maintain stakeholder relationships, while traveling 60% of the time.

As a Senior CRA, you'll monitor clinical trial sites, ensure regulatory compliance, collaborate with teams, and train site staff to maintain standards.

As a Study Support Assistant, you'll assist in study start-up activities, document management, compliance, and team coordination while learning about clinical research.

As a Senior Contract Analyst, you'll manage contractual agreements, ensure compliance, and support project teams in interpreting contracts while maintaining organized records.

As a Manager in Procurement, you will oversee the procurement process, including sourcing, negotiating contracts, and managing suppliers while ensuring compliance and cost-effective operations.

The Senior Site Contract Manager is responsible for reviewing and negotiating contracts, collaborating with teams to assess risks, and maintaining accurate contract records.

As a Senior Contract Analyst, you will manage, analyze, and negotiate contracts, ensuring compliance and supporting project teams while maintaining organized contract records.

The eCOA PM facilitates the use of ePRO and patient technologies, optimizing processes and ensuring compliance in clinical studies while leading stakeholder engagement and project management efforts.

The Financial Accountant II will prepare financial statements, manage financial transactions, ensure compliance, and support budget preparation in a hybrid work setting.