This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA. In this role, you will be involved in the process of supporting clinical trials for various therapies at the country level, and be the liaison between the site and Contract Research Organization (CRO) / Pharmaceutical Company.
Learning Opportunities:
Participate in comprehensive Good Clinical Practice (GCP) Training: Setting you up for success in Clinical Research
Gain knowledge in Clinical Research Industry, Ethics in Clinical Research, Fundamentals of Good Clinical Practice Training, Regulatory Inspection Readiness, Clinical Trial Management System, and Introduction to electronic Trial Master File
Understand Site Activation such as the process of starting up a clinical trial in Singapore, finding the right investigators for a clinical trial in Singapore, regulatory documents collection, review, approval and maintenance of clinical trials regulatory documents
Perform tasks assigned by a manager in either the site activation or site management department, supplemented by soft skills trainings and technical trainings (Trainings may Include: Effective Minute taking during Meetings, Managing Challenging Communications, Cross-cultural Awareness)
Key Requirements:
Bachelor of Science in Life Sciences or Healthcare, Biosciences, Pharmacy related disciplines.
Good interpersonal communication and organizational skills
Good written and verbal communication skills including good command of English
Good word processing skills and knowledge of MS Office applications
Good attention to detail
General awareness clinical trial environment and drug development process
Ability to establish and maintain effective working relationships with co-workers, managers and sponsors
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.
