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Manage Phase 1 clinical research studies, ensuring compliance with protocols and regulations, coordinating logistics, and fostering communication among stakeholders.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

The Associate Director, HR Business Partner provides HR consulting, supports organizational change, and manages HR services aligned with business goals while promoting employee engagement and collaboration across teams.

Manage interdisciplinary clinical research studies, ensuring compliance with regulations, financial performance, and quality of deliverables. Serve as primary liaison between company and customer for timely study conduct.

The Sr Proposal Analyst analyzes RFPs, prepares proposals and budgets, coordinates with SMEs, and manages the proposals process to facilitate project initiation.

Assist in governance meetings, draft minutes, proofread labeling documents, ensure compliance in labeling processes, and manage templates.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

The role involves developing and maintaining R-based applications, mentoring biostatisticians, overseeing projects, and ensuring statistical quality and compliance in clinical trials.

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

Manage clinical trial supplies, ensure compliance with GMP and GCP, oversee vendor management, and maintain project information for studies.