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Oversee RBQM monitoring and risk review strategies, facilitating risk assessments, developing monitoring strategies, and providing oversight to mitigate emerging risks throughout the trial lifecycle.

The Principal Feasibility Analyst conducts feasibility assessments, collaborates with teams, analyzes medical data, and develops strategic reports for clinical trials.

As a Pharmacometrics and MIDD Director, you will lead MIDD, PK, and PD support for projects, analyze relevant data, and mentor team members.

As a Principal Biostatistician, you will lead biostatistical activities, managing clinical trial deliverables and project timelines, while supporting business development and team development efforts.

Provide regulatory guidance for biotech and pharma companies, leveraging expertise in critical therapeutic areas and navigating the regulatory landscape.