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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...

Join us in our exciting journey!!We currently require a motivated, passionate and enthusiastic clinical trials professional to join our team in New Cairo, Egypt!Job OverviewPerform daily administrative activities to ensure a complete and accurate Trial Master File (TMF) delivery.Essential FunctionsAssist local project team members (i.e., CRA, CTA) with...

Job Description: Risk Management LeadRole Title: Risk Management LeadEmployment Type: Full-TimeRole OverviewWe are seeking a strategic and analytical Risk Management Lead to establish, drive, and govern project risk management frameworks across large-scale infrastructure, utilities, and capital projects. In this role, you will lead qualitative and...

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...

About the job: Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. What You'll Do: Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project,...

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)...

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   *...

**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)...

Join our team as a Site Enrollment and Engagement Lead and play a pivotal role in advancing clinical research. This role collaborates with research staff and stakeholders to drive trial recruitment and deliver study-specific training. Acting as a strategic partner, you will optimize site experience and performance while fostering strong relationships...