The Proposals Development Associate will lead client proposal preparation, collaborate with teams, conduct research, manage proposal workflows, and maintain proposal resources.

As a Proposals Writer II, you will develop client-ready proposals, collaborate with experts, and manage project timelines in clinical research.

As a Senior Clinical Data Science Programmer, you will design and implement data pipelines, ensuring data integrity and collaboration with various users in a fully remote environment.

As a Senior Contract Analyst, you will manage contractual agreements, ensure compliance, analyze contract terms, and support project teams to optimize efficiency.

As a Clinical Research Associate II, you will conduct trials, ensure compliance, analyze data, and prepare study documentation in a collaborative environment.

Assist Project Managers in monitoring trials, generate internal and external reports, create study documents, and contribute to process improvement.

The Senior PK Scientist will author clinical pharmacology protocols, perform PK/PD analyses, develop analysis plans, and ensure compliance in clinical trials.

The role involves financial analysis for the Biotech Division, managing study finances, preparing internal and client reports, and forecasting financial performance while collaborating with operational teams for revenue growth.

Oversee the planning, execution, and completion of clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with teams and managing site relationships.

The Business Intelligence Developer will design, develop, and implement BI solutions; collaborate with stakeholders; maintain ETL processes; and create dashboards for insights in healthcare.

As a Financial Analyst II, you will conduct financial analysis, develop models, assist in reporting, and implement process improvements to support business growth.

The Investigator Payments Coordinator manages investigator payments, ensures accuracy, collaborates with departments, escalates issues, and possesses strong system knowledge.

The Workday Lead will manage the Workday product strategy and roadmap, collaborate with HR and IT, and ensure compliance and data integrity within the Workday ecosystem.

The Central Monitor oversees clinical trials, ensuring data quality, implementing monitoring strategies, identifying risks, and improving trial efficiency through data-driven insights.

Oversee and manage clinical trials, ensuring compliance with timelines, budgets, and regulations while collaborating with cross-functional teams and stakeholders.

Lead design, execution, and interpretation of clinical pharmacology studies (PK/PD, exposure-response, modeling/simulation). Integrate pharmacology insights into trial design, guide dose selection, liaise with stakeholders and regulators.

The Investigator Payments Coordinator manages payments to clinical trial investigators, ensures accuracy in financial transactions, and collaborates with teams to support clinical trials.

The role involves developing and validating statistical programs, analyzing clinical trial data, and collaborating with biostatisticians to ensure accurate reporting and compliance with regulations.

As Manager of Financial Business Partnering, you'll steer financial strategy, collaborate with leaders, and drive performance through financial insights and reporting.

Supervise day-to-day sample management operations including receipt, processing, storage, shipment, inventory control, compliance with regulatory/quality standards, cross-functional coordination, and staff training.