The Principal Investigator oversees clinical trials, provides medical oversight, ensures participant safety, and trains study staff while complying with regulatory requirements.

The Key Account Manager drives multi-channel sales strategies, maintains relationships with medical sites, coordinates teams, and optimizes study delivery and performance.

The Principal Investigator oversees clinical trials, ensuring compliance with protocols and GCP, provides medical oversight, and trains staff.

The Principal Investigator oversees clinical trials, ensuring compliance with protocols and GCP, provides medical oversight, and protects participant safety while training staff.

The Senior Specialist oversees training compliance and delegation documentation for clinical research studies, ensuring adherence to regulatory standards and improving operational efficiency through cross-functional collaboration.

The Senior Associate, Operational Excellence will manage site operations, ensure regulatory compliance, lead staff development, and support business growth in clinical research.

Oversee study training compliance and DOA matrix management, ensuring regulatory alignment and operational excellence. Lead a high-performing team to optimize processes and prepare for audits.

Oversee daily warehouse operations, manage inventory levels, supervise staff, ensure compliance with safety regulations, and facilitate collaboration across departments.

The Advisor, Talent Acquisition will enhance sourcing strategies and lead recruiting for PRN positions, mainly phlebotomists and RNs, while managing relationships with healthcare professionals and internal stakeholders.

The Sub Investigator will oversee clinical trial activities, ensure compliance with protocols, manage patient interactions, and assess adverse events, collaborating closely with study teams.

The Technical Project Manager will support project management through planning, coordinating, and monitoring technology solutions for various functional teams, using methods established by the TPM group.

The Specialist coordinates user access and management for clinical systems, monitors compliance, supports onboarding/offboarding, and collaborates with stakeholders to ensure study readiness and system functionality.

As a Specialist in Regulatory Operations, oversee compliance and regulatory activities for clinical trials, particularly for U.S. sites, ensuring adherence to FDA and global standards. Support IRB submissions and maintain essential regulatory documentation.

The Specialist, Regulatory Operations oversees regulatory activities for clinical trials, ensuring compliance and supporting site operations. Responsibilities include managing IRB submissions, regulatory documentation, and collaborating with cross-functional teams.

The Site Manager oversees daily site activities, ensuring protocol compliance for clinical trials, mentoring staff, and managing study tasks and procedures.

Manage Site Support Solutions team, oversee daily operations, hire and train staff, ensure performance metrics are met, and collaborate with leadership and sponsors.

The Senior HR Business Partner will align business strategy with people plans, oversee talent management, ensure compliance in HR practices, and mentor junior HR staff.

The Senior Software Engineer will develop full-stack applications using TypeScript, collaborate with designers, implement APIs, and ensure code quality in a remote setting.

The Senior Specialist in Regulatory Operations will oversee regulatory activities for clinical trials, ensuring compliance with Canadian and USA regulations, and provide support to site operations teams throughout the study lifecycle.

The Senior Data Engineer will design, develop, and maintain data pipelines, optimize data performance, and collaborate with stakeholders to deliver effective data solutions.