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PSI CRO

217 open roles · Clinical

Clinical Research Associate II/I

Full-time
Posted 10 months ago
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Where you can work

Locations named

  • Shanghai, Shanghai, China
  • Beijing, Beijing, China
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Shanghai, Beijing, , China

Role overview

Extracted from the posting. Read the employer’s full description below.

What they are looking for

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 2 years of independent on-site 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
Show all 9 items
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel, up to 70% of time

Employer description

Company Description

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 more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Based in Shanghai/Beijing

Job Description

As a Clinical Research Associate II/I 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 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
  • Prepare and particiapte on audits and inspections

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 2 years of independent on-site 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 problem-solving 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 cross-functional 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
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