Clinical Site Technology Specialist (Nuclear Medicine)
PSI CRO
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 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 sites and provide technical support and expertise related to technology (Kidney imaging, cell therapy, radiology and renal ultrasounds).
You will:
Provide clinical sites with technical support and expertise related to technology (Nuclear medicine, kidney imaging, interventional radiology)
Assist in the design and implementation of study related forms, guidelines and manuals related to technologies
Coordinate data collection related to technologies, including but not limited to nuclear medicine, radiology, etc.
Provide technical and initiation support to sites
Identify, track, and report specific technical timepoints in the study related to study procedures including imaging, scans, and other technologies
Determine technical resources needed for project implementation, and communicates needs to department managers
Organize technical training for project teams
Provide support to the project teams to ensure proper documentation of study-specific assessments related to study technologies
Support site initiation preparation and performs technical visits to assist the site team with technical aspects of the study
Assist and advises the site monitor in the area of study technologies
Provide relevant technology-related information to Business Development for proposals
Prepare for and attends Bid Defense Meetings
Attend and presents at Investigator’s Meetings
Qualifications
BSRT, RN, LPN, and/or equivalent degree
Licensed specialist in relevant technology
Minimum 5 years’ experience in the specified technology: Nuclear Medicine
Experience in operation and QC procedures related to overseeing and managing PET imaging agents and therapeutic RLTs
Proficiency in standard MS Office applications
Must have the ability to travel
Must have excellent communication skills and the ability to collaborate while working in a team environment
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. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.