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The Executive Director leads technology and data initiatives for Site & Study Startup, enhancing operational efficiency and compliance in clinical trials.

Manage design, configuration, launch, monitoring, and close-out of electronic feasibility surveys. Ensure site/investigator readiness, maintain contact lists, track responses and CDAs, apply site identification strategy, and support risk mitigation for global feasibility assessments.

The Senior/Vice President, Technical will lead regulatory strategy initiatives, advise clients on product lifecycles, and represent Parexel as an industry thought leader while mentoring colleagues.

The Vice President, AI Enablement will drive AI strategy and implementation across Parexel, ensuring AI governance, compliance, and integration with business functions, while leading a team of AI professionals.

The Executive Director leads technology and data functions for Clinical Operations, ensuring system reliability, data flow, and process optimization to enhance study execution and operational efficiency.

The Clinical Laboratory Study Manager manages clinical trial sample operations, ensures compliance, oversees data management, and liaises with various stakeholders to support biomarker evaluation.

The Investigator Contracts Lead negotiates contracts and budgets with clinical sites, manages the site contracting process, and oversees contracting teams to ensure compliance and timely execution of agreements.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.

The Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.