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The Scientist III supports laboratory operations by maintaining LC-MS instruments, troubleshooting issues, and performing LC and LC-MS analysis for investigational compounds.

The Study Start Up Project Manager leads global start up strategy, coordinating with various teams to activate study sites and ensure compliance, quality, and timely completion of clinical trial start up activities across multiple therapeutic areas.

The Start Up Project Manager II leads global project strategies for clinical studies, managing site activations and coordinating with cross-functional teams to ensure timely and efficient project delivery across various therapeutic areas.

As a Clinical Research Associate at Parexel, you will participate in clinical trials and contribute to regulatory processes, ensuring optimal health outcomes.

The Clinical Research Associate is responsible for site management, monitoring clinical studies, ensuring compliance with regulations, and supporting site staff in study-related matters.

The Global Site Start Up Leader manages the execution of site activation for clinical trials, develops strategies, ensures compliance, and leads cross-functional collaboration while meeting project timelines.

The Regulatory Affairs Consultant will manage the labeling lifecycle, ensure compliance with regulations, prepare documents for submissions, and support labeling initiatives in a global team.

The Associate Director, Data Engineering is responsible for facilitating data movement within the Enterprise Data Lake, overseeing data engineering activities, and leading cross-functional teams. The role includes strategic contributions to data lake architecture, data governance, and the development of operational data products in various domains while managing and mentoring data engineering teams.

The Clinical Finance Analyst II is responsible for managing clinical financial processes, including invoice processing, account reconciliation, and quality control, while supporting finance relationships and providing budget analysis and reports.

The Site Contract Associate II is responsible for negotiating, finalizing, and executing site contracts and ensuring compliance with regulatory requirements while maintaining relationships with trial sites.