Clinical Research Regulatory Expert

Clinical Project ManagerOverview:The Clinical Project Manager will oversee the strategic planning, execution, and completion of assigned clinical research projects.Responsibilities:Manage project planning, execution, progress, and completion to ensure timely delivery and quality outcomes.Collaborate with functional experts to ensure compliance with...

**Unit Management**: - Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites. - Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current...

Job Title: Clinical Research Project CoordinatorThe role of a Clinical Research Project Coordinator is to ensure the successful initiation, planning, execution, monitoring, controlling, and closure of assigned early-phase clinical research projects. This includes operational management and oversight of clinical investigative sites as well as clinical...

The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions comply with applicable regulations and internal timelines.More specifically, the...

The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst and Programmer will be responsible to gather, understand and analyze the needs reported by the Data...

Job Title: Clinical Project ManagerAbout the RoleThis is a challenging role that involves overseeing clinical research projects from initiation to completion. You will work closely with cross-functional teams to ensure all project activities align with regulatory requirements, industry standards, and organizational policies.Main Responsibilities:Plan,...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

Job Description:">The Site Selection Specialist is a vital member of the project team, serving as the primary point of contact for site selection activities. This includes identifying and evaluating potential research sites to ensure they meet specific criteria.">This role is perfect for those with experience working in clinical research, particularly in...

**Project Management**: - Manage the planning, execution, progress and completion of assigned clinical research projects. - Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies. - Maintain operational, financial and regulatory integrity and safety. - Develop and/or participate...

**Project Management**:- Manage the planning, execution, progress and completion of assigned clinical research projects.- Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.- Maintain operational, financial and regulatory integrity and safety.- Develop and/or participate in the...