Job Description
🌍 Join Our European Clinical Research Network!
Agile Clinical Trendz is expanding its network across the DACH Region (Germany, Austria, and Switzerland) and is looking for experienced Clinical Research Consultants to support upcoming Real-World Evidence (RWE), observational, and multicentre clinical research projects.
We are currently seeking professionals with experience in:
✅ Clinical Research Associates (CRAs)
✅ Clinical Research Coordinators (CRCs)
✅ Clinical Trial Specialists
✅ Site Operations Professionals
✅ Clinical Project Coordinators
✅ Feasibility Specialists
✅ Site Start-Up Specialists
✅ Ethics & Regulatory Submission Specialists
✅ Clinical Data Collection / Chart Review Specialists
✅ Clinical Research Consultants
✨ Why Join Agile Clinical Trendz?
Flexible consulting opportunities
Work on international clinical research projects
Collaborate with global pharmaceutical and biotechnology companies
Build long-term professional partnerships
Contribute to impactful research across Europe
Agile Clinical Trendz is expanding its network across the DACH Region (Germany, Austria, and Switzerland) and is looking for experienced Clinical Research Consultants to support upcoming Real-World Evidence (RWE), observational, and multicentre clinical research projects.
We are currently seeking professionals with experience in:
✅ Clinical Research Associates (CRAs)
✅ Clinical Research Coordinators (CRCs)
✅ Clinical Trial Specialists
✅ Site Operations Professionals
✅ Clinical Project Coordinators
✅ Feasibility Specialists
✅ Site Start-Up Specialists
✅ Ethics & Regulatory Submission Specialists
✅ Clinical Data Collection / Chart Review Specialists
✅ Clinical Research Consultants
✨ Why Join Agile Clinical Trendz?
Flexible consulting opportunities
Work on international clinical research projects
Collaborate with global pharmaceutical and biotechnology companies
Build long-term professional partnerships
Contribute to impactful research across Europe
Requirements
Preferred Qualifications:
✔ Clinical research experience within Europe
✔ Good Clinical Practice (ICH-GCP) knowledge
✔ Site feasibility and site management experience
✔ Ethics Committee and Regulatory submission experience
✔ Clinical Operations and Project Coordination experience
✔ Medical record abstraction and eCRF/EDC knowledge
✔ Fluency in one or more relevant languages (German and English preferred; French or Italian is an advantage)
✔ Clinical research experience within Europe
✔ Good Clinical Practice (ICH-GCP) knowledge
✔ Site feasibility and site management experience
✔ Ethics Committee and Regulatory submission experience
✔ Clinical Operations and Project Coordination experience
✔ Medical record abstraction and eCRF/EDC knowledge
✔ Fluency in one or more relevant languages (German and English preferred; French or Italian is an advantage)