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Provide project related assistance for all assigned project(s) sites and project teams. Ensure all work is conducted in accordance with SOPs policies and practices good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
Essential Functions
Perform processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
Task may be assigned on either StartUp studies or Maintainance studies.
Establish and maintain effective project/ site communications
Create and maintain relevant project documents
Ensure accurate completion and maintenance of internal systems databases tracking tools timelines and project plans with project specific information
Review evaluate and recommend modifications to designated processes
Participate in document management (creation review maintenance storage as applicable)
Participate in (study) team meetings and implement action items
Collaborate with the project lead/team members in creation/review of study documents
Setting quality standards and reviewing deliverables to the same for process tasks.
Work on visit tracking in CTMS for Investigator payments Vendor Setup QCs PV Batch Review Passthrough invoice Batch Review & associated tasks.
Providing and revoking access .
Review ATP (Authorization to proceed) trainings.
Cordinating with translation vendors.
Understanding the contracts & enabling excellent output quality for the processing teams.
Ensure effective and efficient coordination between the operations team (PM/RSU/Clinical/IPA) for visit/passthrough batch query resolutions.
Ability to work in a deadline orientated environment and manage SLAs (TAT Productivity Quality) effectively.
Respond to adhoc requests for data/information/analysis.
Responsibile for general administrative support for projects tracking various kinds of activities.
Responsible for indexing.
May act as a buddy for new Hires and SME for the team
Qualifications
Bachelors Degree Pref
Life Sciences graduates with minimum 2 years relevant experience. Pref
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
Full-Time