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Responsible for supporting clinical trials through logistical set up, data compilation, and participant coordination. Ensures compliance with protocols and maintains participant safety.

The Payment Manager I prepares grants forecasts, analyzes budgets, collaborates with teams for accurate reporting, and supports process improvements in grant payment systems.

The Site Budget & Contracts Specialist prepares site budgets, negotiates Clinical Trial Agreements, and collaborates with legal and clinical personnel to ensure compliance during the contract negotiation process.

Support the Clinical IT Platform team with projects, media content creation, client meeting preparation, and daily operations in a dynamic environment.

Manage clinical trial budgets and contracts, ensuring timely execution and efficiency in study start-up processes while improving service delivery methodologies.

The Associate Medical Data Review Manager ensures execution of Central Medical Review activities, collaborating across teams, analyzing data for patient safety, and overseeing the configuration and use of medical review tools.

As a Senior Biostatistician, you will design, analyze, and interpret clinical trials, ensuring the quality of statistical deliverables and collaborating with cross-functional teams.

The QA Lead oversees quality issues in the QMS, tracks case timeliness, supports teams in CAPA creation, and ensures effective communication of quality matters.

The role involves reviewing and implementing necessary compliance documents, ensuring data entry compliance, and managing documentation for clinical studies, emphasizing strong attention to detail and communication skills.

The Proposal Manager II coordinates proposal processes, engages stakeholders, manages timelines, and ensures high-quality, client-focused proposals, while overseeing deliverables and team workload in a fast-paced environment.