Senior Clinical Project Manager, Early Phase Oncology (UK/Europe, Home-based) - IQVIA Biotech

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ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONS for all activities related to implementation of clinical studies projects of full scope regional and global projects.  Responsible for project team leadershipResponsible for building and maintaining positive client relationshipsAbility to negotiate with clients to assure IQVIA Biotech’s operational processes are maintained, projects are done within scopeReviewing and identifying project study trends and proactively responding to client and respective team membersDeveloping appropriate early warning systems of potential obstacles to the successful completion of the projects; analyzes information and develops innovative solutions to challengesIdentifying, define, document training requirements in LMS systems and assure project level compliance with study specific training requirementsResponsible for change management on all assigned projectsResponsible for assuring projects assigned are run according to SOPs and WP as refined in the contractResponsible for assuring project timelines are met as per contractResponsible for identifying processes which need updating and documenting that to the direct line manager or divisional leadResponsible for maintaining client relationships for all assigned work, keeping all project reporting current, and assuring executive management is awareIn conjunction with management, assists with developing, documenting, and updating internal processes and processes required for consistency across programs such as SOPs, working practices, and related quality assurance forms.Provide other project support to Managers, as assignedOversee delegation of support staff activities, as necessaryAssists in the development and delivery of capability and proposal defense presentations to prospective clientsSupports Contracts and Proposals with final project contract execution and CIS documentation by the project team.  Represents senior management in negotiation of contracts as appropriate.Participates in the performance appraisal program by providing timely and accurate feedback regarding the performance of respective team members at least annuallyMaintains current knowledge of FDA regulations, and GCP and ICH Guidelines for clinical research.Responsible to maintain personal currency documentation for IQVIA Biotech SOPs, CAPA completion and timesheet maintenance including assurance or back-up PM staff at every instance of out of office#LI-JS2#LI-RemoteAt IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at .Full time

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