PSI is a leading Contract Research Organization with more than 30 years 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- 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.
- Previous experience (5+ years) as a nuclear medicine technologist
- Experience in operation and QC procedures related to the equipment used in the specialized area
- MRI experience preferred
- Clinical trial experience is a plus
- RN, LPN, or equivalent associate degree
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.
What We Do
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
