Job 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 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

As a Site Technology Specialist, you will work with clinical trial sites to provide technical support and expertise related to imaging/radiology, including radionuclide/radioligand therapy and cell therapy operations - collectively referred to as "technology".

This position is based in Japan ( Tokyo or Osaka ) 

You will:

1. Determine technical resources needed for project implementation, and communicates needs to department managers

1. Assist in the design and implementation of study related forms, guidelines and manuals related to technologies

1. Organize technical training for project teams

1. Assist and advises the site monitor / CRA in the area of study technologies

1. Assist with clinical trial sites' technology equipment qualification surveys

1. Support site initiation preparation and performs technical visits to assist the clinical trial site team with technology aspects of the study

1. Provide technical and application training and support to clinical trial sites throughout the project lifecycle

1. Provide real-time support to clinical trial sites to correct image quality issues

1. Coordinate data collection and resolution of queries related to technologies, including but not limited to nuclear medicine, radiology, cell therapy operations, etc.

1. Identify, track, and report specific technical timepoints related to study procedures including imaging/scans, and other technologies

1. Provide support to ensure proper documentation of study-specific assessments related to technologies

1. Provide relevant technology-related information to Business Development for proposals

1. Prepare for and attends Bid Defense Meetings

1. Attend and presents at Investigator’s Meetings

Qualifications

Qualifications

I. Education:

Bachelor's degree in any of the following (or equivalent), preferably with specialization in Nuclear Medicine Science / Nuclear Medical Technology:

-Medical Radiation Science

-Medical Radiologic Technology

-Medical Technology

-Diagnostic Radiography

-Diagnostic Imaging and Radiotherapy

-Biomedical Imaging and Radiation Science

II. Experience:

• Licensed specialist in relevant technology. 
• Minimum 3 years’ experience as Nuclear Medical Technologist (NMT) or similar role.
• Must have performed clinical nuclear medicine tasks, including but not limited to experience in operation and QC procedures related to overseeing and managing PET imaging agents and therapeutic RLTs.
• Prior exposure in clinical trial conduct. (e.g., Clinical Application Specialist or similar role) will be of added advantage
• Cultural intelligence to support diverse countries within the APAC region with sensitivity and understanding international mindset to work collaboratively with department team members in the global community.
• Effective communication and stakeholder management skills to foster collaboration and managing relationships effectively within a matrix team setting.
• Capable of working independently and taking initiative to drive tasks forward.
• Skilled in tackling unstructured and complex challenges with innovative solutions. 
• Comfortable navigating and thriving in dynamic and at times ambiguous environments.
• Some work travel may be expected for this regional role.

III. Language

Japanese: Business level

English: Business level

Additional Information

Take the next step in your career and join a company that genuinely focuses on its people.

About Us

PSI is a passionate, organically grown, and award-winning full-service CRO who dares to be different. As a dynamic and global company, we bring together dedicated experts across 60 countries working collectively to help make a positive impact on patient lives.

How are we different?

PSI is privately owned by the very people who founded the company almost 30 years ago, and they’re still working here today. As a result, we have grown organically around the globe and have kept our company fully independent, giving us significant advantages and freedoms.

Being a Part of the Team

As a part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents.

You will receive continuous support from your global peers and join a fast-paced, innovative, and results-oriented working environment with lean communication lines. We pride ourselves on being approachable, receptive to new ideas, and open to feedback.

Growth Opportunities

PSI is proud to invest in our people, from entry-level team members to senior leaders, helping you identify and hone your unique strengths at every step of your career. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.

The PSI Advantage 

PSI CRO has been named a 2022 CRO Leadership Award Champion in the categories of Compatibility, Quality, and Reliability across two respondent groups (Overall and Small Pharma). This is the fourth year in a row that PSI CRO received CRO Leadership Awards in all 5 categories, also including Expertise and Capabilities. The CRO Leadership Awards are presented by Life Sciences Leader and Clinical Leader based on research conducted by ISR reports. The awards recognize CROs that are voted by sponsors to meet or exceed expectations.

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