Imaging Research Associate I

Clario’s medical imaging expertise is unparalleled to any other medical imaging core lab in the industry, and we're looking to hire Imaging Research Associates for our growing Imaging Operations team in Budapest.

Please note that this is a fixed-term position, with the contract set to conclude upon the employee's return from maternity leave. The role offers a unique opportunity to join our dynamic team and contribute meaningfully during this time.

What we offer:

• Competitive compensation

• Attractive benefits (security, flexibility, support and well-being)

• Engaging employee programs

• Flexible hybrid working model

• OTP Szép Card

What you'll be doing:

• Study Coordination: Oversee site activities from start to finish, ensuring timely delivery of study deliverables. Assist with study start-up tasks, including preparation of study materials and scheduling site training.

• Data Management and Quality Control: Review, process, and monitor study-related data. Resolve data discrepancies, manage internal quality control (IQC) processes, and ensure accurate tracking of data and equipment.

• Site Communication and Reporting: Manage communications with clinical sites and sponsors. Generate and verify reports, track project progress, and address logistical issues.

• Project Support: Assist Project Managers with site start-up, project administration, and maintaining project timelines. Monitor data flow, identify trends, and recommend actions for project improvement.

• Client Relations and Compliance: Respond to client inquiries professionally, maintain client satisfaction, and adhere to Standard Operating Procedures (SOPs). Participate in modifying SOPs and upholding departmental standards.

• Continuous Learning: Stay updated with technical and industry knowledge through company-sponsored training sessions.
   

What we look for:

• Associate/Bachelor's Degree in bioscience, computer science, information technology or related field preferred

• Familiarity with standard software packages including e-mail, word processors, Excel spreadsheets and databases

• Knowledge of the drug development/clinical trials process and/or experience working in a pharmaceutical environment preferred

• Knowledge of “good clinical practices” preferred

• Ability to work in group setting and independently; ability to adjust to changing priorities

• Excellent attention to detail and orientation toward meticulous work

• Strong interpersonal and communication skills, both verbal and written

• Ability to provide and maintain a professional and positive attitude

• Leadership skills. Self-motivated with ability to work in teams with minimal supervision, with aggressive deadlines

• Strong documentation and organizational skills

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.