Clinical Research Associate II
PSI CRO AG · Taipei, Taiwan · full-time · Hybrid · 7 days ago
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Job Description
We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Taiwan. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Why join PSI?
- Established global CRO with a strong reputation for high client retention and long-term partnerships
- Collaborative, relationship-driven culture focused on sustainable client success
- Supportive and stable environment with one of the industry’s lowest staff turnover rates
- Clear and structured career development pathways to support long-term growth
What we offer
At PSI CRO AG', we are committed to providing a supportive and enriching work environment for our employees. This role offers excellent opportunities for professional development, including training and mentorship programs. You will also enjoy a competitive salary, comprehensive benefits package, and the chance to be part of a dynamic, global organisation at the forefront of clinical research.
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Facilitate site budgets and contract negotiations
- Monitor trial progress on the country level
- Be responsible for site communication and management
- Be a point of contact for in-house 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
Qualifications
- College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
- At least 2-3 years of independent on-site monitoring experience in Taiwan
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases (preferable)
- Full working proficiency in English and Chinese
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
- Employer
- PSI CRO AG
- Location
- Taipei, Taiwan · Hybrid
- Contract
- full-time