Offer summary

Qualifications:

Bachelor's Degree in Life Sciences or a related field., Familiarity with PC-based software including email, Word, Excel, and databases., Knowledge of drug development, clinical trials, or experience in a pharmaceutical environment is preferred., Understanding of good clinical practices is advantageous..

Key responsibilities:

Oversee site activities from start to finish, ensuring timely study deliverables.

Review, process, and monitor study data, resolving discrepancies and managing quality control.

Manage communication with clinical sites and sponsors, generate reports, and track project progress.

Assist project managers with site start-up, project administration, and maintaining timelines.

Job description

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 Imaging Operations team in Budapest.

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:

Bachelors Degree in Life Sciences or similar
Familiarity with PC-based computers and standard software packages including e-mail, word processors, Excel spreadsheets and databases.
Knowledge of the drug development/clinical trials process/basic clinical research and/or experience working in a pharmaceutical environment preferred
Knowledge of “good clinical practices” preferred

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.

Required profile