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Job Description Summary -Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against...

Job Description Summary-Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against...

About the job The Clinical Project Manager II (CPM II) is responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM II is expected to perform most tasks independently but still requires support and guidance of the trial assigned...

About the job The Clinical Project Manager (CPM) is responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM is expected to perform most tasks independently but still requires support and guidance of the trial assigned Director...

Line of ServiceAdvisoryIndustry/SectorTechnologySpecialismAdvisory - OtherManagement LevelManagerJob Description & SummaryA career in our Enterprise Risk Management practice, within Risk and Compliance services, will provide you the opportunity to work with a team that provides clients with extensive risk and controls technical knowledge and sector specific...

What You'll Do: Assist/Advise project teams on all regulatory requirements for clinical studies  Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings  Review and adapt study specific documents according each country and site requirements   Perform IRB/EC (CA)...