We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

PSI's business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients.

We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here.

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.

Office-Based in Taipei

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.

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.

Clinical Research Associate II