As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.
You will:
- Conduct and report SSV SIV RMV COV onsite monitoring visits
- Perform CRF review source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for inhouse support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and particiapte on audits and inspections
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- At least 23 years of independent onsite monitoring experience in China
- Experience in all types of monitoring visits in Phase II and/or III
- Therapeutic area experience in Oncology is a plus
- Full working proficiency in English and Mandarin
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problemsolving skills
- Ability to travel up to 70% of time
Additional Information :
Advance your career in clinical research overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated crossfunctional teams get all support and ownership of your projects.
- Excellent working conditions
- Extensive training and friendly collegial team
- Competitive salary package
- Opportunities for personal and professional growth
Remote Work :
No
Employment Type :
Fulltime