Clinical Trials Associate

IQVIA; Singapore; On-site; SGD 100,000 - 125,000; Full time

Job summary

A leading clinical research organization in Singapore is offering a unique opportunity for graduates to support clinical trials and be trained by professionals. You will assist in various tasks, including site activation and management processes, while gaining significant knowledge in clinical research practices and regulations. Candidates must possess a Bachelor of Science in Life Sciences or similar, along with strong communication, organizational, and word processing skills. This role is a fantastic starting point for a career in clinical research.

Qualifications

• Bachelor's degree in a relevant field such as Life Sciences or Pharmacy.
• Strong interpersonal and organizational skills.
• Good command of English, both written and verbal.

Responsibilities

• Support clinical trials for various therapies at the country level.
• Liaise between the site and Contract Research Organization / Pharmaceutical Company.
• Participate in GCP training and various soft skills trainings.

Skills

Interpersonal communication

Organizational skills

Attention to detail

Written communication

Verbal communication

MS Office skills

Education

Bachelor of Science in Life Sciences, Healthcare, or Pharmacy

Job description

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