
Clinical Research Associate
3 days ago
Company Description
PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
**Job Description**:
**You will**:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup (if applicable)
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Supervise study activities, timelines, and schedules on the country level
- Be a point of contact for in-house support services and vendors
- Be involved in quality control, such as compliance monitoring and reports review
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
**Qualifications**:
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- At least 1-2 years of on-site monitoring experience in Singapore
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology studies
- Full working proficiency in English
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Additional Information
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
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