Associate Clinical Project Manager
PharmaCROBiotechClinical ResearchQuality Assuranceinform
Job description
Oncology experience a plus but not required. PURPOSE Assist in the execution of the assigned regionally-based clinical study(ies) per Contract, from initiation through to closeout. Support all clinical study related activities for assigned projects in accordance with SOPs, policies and practices, meeting quality and timeline metrics. RESPONSIBILITIES Vendor Management; contracting, finances, trouble shooting. Create, track and report on project timelines. Produce and distribute status, tracking and financial reports for internal and external team members and senior management. Assist the clinical project manager(s) with budget allocation and approval of invoices. Serve as primary back up project contact with Sponsor and internal project team to ensure communication is maintained and reporting schedules are adhered to. Identify out of scope project work. Escalate findings and action plans to appropriate parties. Coordinate data gathering for the development of proposals for new work. Prepare and present project information at internal and external meetings. Coordinate with other project support staff within and outside the Clinical Project Management Unit to identify and consolidate support processes. Undertake clinical project management activities as directed by Clinical Project Manager. Train and may coordinate the work of more junior project support staff. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Finance Analyst (Clinical Trials)
Thermo Fisher Scientific — Sofia, Bulgaria
ManufacturingTechnician Finishing - 3rd Shift
Thermo Fisher Scientific — Grand Island, New York, USA
Project Manager II
Thermo Fisher Scientific — Florence, South Carolina, USA
Market Development Manager, AI Scientific Platform
Thermo Fisher Scientific — 8 Locations
Senior/Principal - Country Approval Specialist
Thermo Fisher Scientific — Remote, North Carolina, USA
Lead Biostatistician - Pharmacovigilance (PV) Focus
Thermo Fisher Scientific — 2 Locations