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The CRA II conducts site monitoring, compliance checks with regulations, and supports site management during clinical trials, ensuring quality data and patient safety.

The Sr Product Ops Analyst collaborates on Oracle PPM solutions, supports data migration, develops test scripts, and provides training and insights on project performance.

The CRA II conducts monitoring of clinical research studies, ensuring compliance with regulations, managing project components, and supporting trial operations.

The CRA I is responsible for site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulations and protocols while supporting subject recruitment and project goals.

The Clinical Trial Manager oversees site management, monitoring, risk assessment, team coordination, and compliance to ensure successful clinical trial execution.

The Principal Product Manager will define product vision, align teams, analyze markets, oversee product lifecycles, and ensure customer needs are met while leading and mentoring other product managers.

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.

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.

Responsible for site activation, compliance with project timelines, reviewing documentation, and liaising between sites and teams to ensure regulatory submission success.

The Sr. SAS role involves collaborating within the Clinical Solutions team to accelerate drug development and support customer success in complex environments.