PURPOSEEngage in company training program to gain knowledge and skills required to provide administrative support to projects in accordance with SOPs, policies, good clinical practices, and applicable regulatory requirements. Meeting quality and timeline metrics under direction of line manager and/or other designated team members.RESPONSIBILITIESComplete appropriate role-specific training to perform job duties.Under supervision, perform assigned administrative tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, preparing and distributing status reports, creating and maintaining study documents, etc.).Under supervision, assist in updating and maintaining systems within project timelines/plans.Perform the activities as per the task list delegated by Centralised Monitoring Specialist/Centralized Monitoring Lead.REQUIRED KNOWLEDGE, SKILLS AND ABILITIESBasic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations, and guidelines.Exposure to MS Applications including but not limited to Microsoft Word, Excel and PowerPoint.Effective written and verbal communication skills including good command of English language.Effective time management skills.Results and detail-oriented approach to work delivery and output.Ability to establish and maintain effective working relationships with coworkers, managers and clientsStrong listening and phone skills.Good data entry skills.MINIMUM REQUIRED EDUCATION AND EXPERIENCEGraduate/Post Graduate in Life Sciences or educational equivalent up to 6 months of relevant experience; or equivalent combination of education, training and experience.Experience level may vary based on customer specific requirementsIQVIA 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 atIQVIA 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.
