Clinical Trial Assistant (m/f/d)

office-based in Dresden | permanent position | full-time or part-time

We want to expand our young, dynamic and growing CTA team and are therefore looking for new talent and experienced specialists preferably on a full-time basis.

About us:

ABX-CRO is an internationally operating contract research organization headquartered in Dresden. We provide global services in the manufacturing, testing, and regulatory approval of pharmaceuticals and diagnostics. Our core expertise lies in nuclear medicine drug development, with a strong focus on radiopharmaceuticals for both therapeutic and diagnostic applications.

Our CTA team supports the planning, coordination, and execution of clinical trials. We are currently seeking reinforcement to support the coordination of tasks within the imaging area (Image Core Lab).

This is what you do as a CTA with us:

• Operational support for the Image Core Lab study team in coordinating and conducting clinical trials in accordance with ICH-GCP
• Maintenance of trial master files
• Support in preparing and completing study-related documentation
• Collaboration with cross-functional teams to facilitate and ensure the smooth conduct of clinical trials
• Oversight of relevant training
• Organisation and follow-up of meetings
• Support and preparation of audits and inspections
• Communication with trial centres, external partners and sponsors
• Assistance with tracking and reporting key figures and milestones for clinical trials

Must-haves

• Professional training as a medical documentalist or documentation assistant, medical-technical radiology assistant, medical assistant or similar qualification
• Experience in working with imaging techniques
• Structured, reliable and independent working style
• Flexibility, organisational skills, willingness to work in a team and initiative
• Good English skills & very good communication skills
• Confident use of MS Office package

Nice to have

• Professional experience as a study nurse, CTA, CRA or in related fields of clinical trial administration
• Experience with radiopharmaceuticals in clinical research
• Knowledge of ICH GCP guidelines
• Initial experience with clinical trial software (eCRF, eTMF, CTMS, etc.)