Summary

PSI CRO is a leading global contract research organization (CRO) specializing in full-service clinical development for pharmaceutical and biotechnology companies. Founded in 1995, PSI has established itself as a prominent player in the clinical research industry with operations spanning across North America, Europe, Asia, and Australia. The company focuses on delivering high-quality clinical trial services with particular expertise in oncology, central nervous system disorders, infectious diseases, and rare conditions. PSI's operational model emphasizes therapeutic expertise, operational excellence, and a patient-centric approach to clinical research. With a team of experienced professionals, the company manages all phases of clinical development from study design and protocol development to regulatory submissions and post-marketing studies. PSI is known for its efficient study execution, robust quality management systems, and commitment to accelerating drug development timelines while maintaining rigorous scientific standards.

Job description

Job Description

Provides clinical sites with technical support and expertise related to technology.
Assists in the design and implementation of study related forms, guidelines and manuals related to technologies.
Coordinates data collection related to technologies, including but not limited to nuclear medicine, radiology, etc.
Provides technical and initiation support to sites.
Identifies, tracks, and reports specific technical timepoints in the study related to study procedures including imaging, scans, and other technologies.
Determines technical resources needed for project implementation, and communicates needs to department managers.
Organizes technical training for project teams.
Provides support to the project teams to ensure proper documentation of study-specific assessments related to study technologies.
Supports site initiation preparation and performs technical visits to assist the site team with technical aspects of the study.
Assists and advises the site monitor in the area of study technologies.
Provides relevant technology-related information to Business Development for proposals.

Qualifications

Experience as a nuclear medicine technologist
Previous experience in diagnostic imaging
Clinical trial experience is a plus
Associate degree required, bachelor's degree preferred

Requirements

Experience as a nuclear medicine technologist
Previous experience in diagnostic imaging
Clinical trial experience is a plus
Associate degree required
Bachelor's degree preferred
Must not require work visa sponsorship

Company overview

PSI CRO is a leading global contract research organization (CRO) specializing in full-service clinical development for pharmaceutical and biotechnology companies. Founded in 1995, PSI has established itself as a prominent player in the clinical research industry with operations spanning across North America, Europe, Asia, and Australia. The company focuses on delivering high-quality clinical trial services with particular expertise in oncology, central nervous system disorders, infectious diseases, and rare conditions. PSI's operational model emphasizes therapeutic expertise, operational excellence, and a patient-centric approach to clinical research. With a team of experienced professionals, the company manages all phases of clinical development from study design and protocol development to regulatory submissions and post-marketing studies. PSI is known for its efficient study execution, robust quality management systems, and commitment to accelerating drug development timelines while maintaining rigorous scientific standards.