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As a Clinical Research Associate II, you will conduct clinical trial visits, ensure compliance, collaborate with investigators, and perform data reviews.

The Trial Project Manager oversees the planning, execution, and delivery of clinical research projects, ensuring objectives are met on time and within budget.

As a Clinical Research Associate II, you will conduct clinical trial visits, ensure protocol compliance, review data, and collaborate with site staff.

As a Senior Statistical Programmer, you will build and validate statistical programs, lead programming deliverables, and ensure compliance with global trial regulations.

As a Clinical Research Associate II, you will conduct clinical trial visits, ensure protocol compliance, collaborate with site staff, and perform data analysis.

As Manager of Financial Business Partnering, you will provide strategic financial insights, manage budgeting, and collaborate with business leaders to enhance financial performance.

The Senior Statistical Programmer performs SAS programming for clinical trial data analysis, ensuring data integrity, quality control, and support for regulatory submissions while mentoring junior team members.

The Site Specialist II supports site activation tasks ensuring compliance with regulations, oversees document processing, and coordinates project activities and communications with stakeholders.

As a Senior Statistical Programmer, you'll lead programming for clinical studies, develop ADaM datasets, mentor junior staff, and ensure compliance with quality standards.

As a Clinical Research Associate, you will conduct and monitor clinical trials, ensuring protocol compliance, data integrity, and patient safety. Collaboration with site staff and data management is key.