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The Sr. TMF Specialist processes study documentation, ensures compliance, manages TMF repositories, performs quality checks, and trains junior staff.

Oversee clinical research projects, ensuring compliance with protocols, managing regulatory activities, recruiting participants, and maintaining quality control while supporting the Principal Investigator.

Coordinate clinical research projects by planning, conducting, and overseeing activities, ensuring compliance with regulations and maintaining study documentation.

The Senior Proposal Writer leads proposal strategy development, collaborates with stakeholders, creates customized proposals, coaches junior writers, and manages timelines to meet customer needs.

Perform data entry, tracking, verification, and quality control checks for a clinical trial database while maintaining confidentiality. Assist with system improvements and training material preparation.

The Data Entry Specialist performs accurate data entry and verification, identifies technical issues, maintains data integrity, and assists with system improvements for clinical research processes.

The Exec Director will define and execute cloud strategies, manage multicloud operations, oversee infrastructure, drive cost optimization, ensure security compliance, and lead a global team.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

Coordinate clinical research projects, manage study documentation, ensure compliance with regulations, and facilitate participant recruitment and monitoring activities throughout clinical trials.

The Internal Account Director develops and implements recruitment and retention strategies, collaborates with teams to meet customer goals, and analyzes market trends for product improvements.