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The Sr. Site Contracts Specialist leads contract negotiation and management for clinical trials, ensuring compliance and fostering collaboration with stakeholders. Responsibilities include preparing contracts, managing budgets, and training junior staff, while maintaining project timelines and quality standards.

Manage external budgets and contracts for clinical trials, ensuring alignment with regulations, and providing financial expertise to stakeholders.

The IMS Specialist II processes investigator payments, coordinates with internal teams, maintains financial records, and provides guidance during the grants payment process, while ensuring compliance with agreements and audits.

Manages clinical research projects ensuring compliance with regulations, oversees project delivery, maintains budgets, and develops client relationships.

Lead statistical programming for clinical trials using R and SAS to produce tables, listings, and figures per SAP. Manage and mentor programmers, ensure CDISC compliance (SDTM/ADaM), maintain documentation, perform validation/QC, and support regulatory submissions while following SOPs and regulatory guidelines.

The Sr. Biometrics Data Engineer will architect, implement, and maintain scalable ETL pipelines, manage data ingestion, and collaborate across teams to ensure robust data infrastructure.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

The Principal Statistical Programmer develops programming code using SAS to generate datasets, summary tables, and graphs, while ensuring quality and compliance with standards, manages project documentation, and mentors junior staff.

The Clinical Scientist contributes to protocol design, scale management, and provides training on clinical scales while ensuring data consistency and performing statistical analysis.

The Site Activation Specialist II/Sr. will manage site start-up activities, including regulatory submissions, contract negotiations, and site communication to ensure efficient clinical trial initiation and compliance with quality standards.