All jobs
PSI CRO logo
PSI CRO

200 open roles · Clinical

Clinical Research Associate II

Full-time
Posted 1 week ago
Apply on company siteYou’ll apply directly with the employer on SmartRecruiters.
Added to ZestAmigo
Last seen on employer site

Where you can work

Hybrid

2 workplaces

  • Tokyo, Tokyo, Japan
  • Osaka, Osaka, Japan
View location wording from the posting
Tokyo/Osaka, , Japan

Role overview

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

What they are looking for

  • Office is based in Japan. Tokyo or Osaka office (Hybrid)
  • College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
  • Min. 2 years of independent on-site monitoring experience in Japan
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in feasibility assessment and study set-up process is preferable
Show all 11 items
  • Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
  • Full working proficiency in English and Japanese
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel up to 30% to 40%

Employer description

Company Description

PSI is a leading Contract Research Organization with more than 30 years of experience 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

We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Japan. 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.

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

Office is based in Japan. Tokyo or Osaka office (Hybrid)

  • College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
  • Min. 2 years of independent on-site monitoring experience in Japan
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in feasibility assessment and study set-up process is preferable
  • Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
  • Full working proficiency in English and Japanese
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel up to 30% to 40%

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Track this application

Keep your own notes. Only you can mark an application as sent.

Report a problem with this listing

Sign in to report this listing.

More at PSI CRO

Hybrid

Budapest, Budapest, Hungary

Full-time

Salary unavailable

Posted 2 months ago

Source: SmartRecruiters