Clinical Trials Associate
2 weeks ago
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 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
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