Clinical Trial Associate (Germany)
at UCB
Monheim, Bayern, Germany -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 01 May, 2025 | Not Specified | 02 Feb, 2025 | 2 year(s) or above | Regulatory Requirements,Clinical Research | No | No |
Required Visa Status:
| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
| GC Green Card |
Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
MAKE YOUR MARK FOR PATIENTS
We are looking for a Clinical Trial Associate (Part-Time -50%) who is detail-oriented, organized, and proactive to join us in our Clinical Operations team, based in our office in Monheim, Germany.
ABOUT US
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.
ABOUT US
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Responsibilities:
ABOUT THE ROLE
You will be working in a team that supports the planning, execution, and management of clinical trials. You will be responsible for maintaining trial documentation, coordinating with study sites, and ensuring compliance with regulatory requirements. A key focus will be on onboarding Contract Research Organizations (CROs) with relevant accesses and training and coordinating sponsor activities.
WHAT YOU’LL DO
- Onboard CROs incl. set-up of SOP lists, training matrix, user account creation and management, assist with CRO access to UCB systems, e.g. Veeva vaults
- Assist in the preparation and maintenance of trial documentation within the Veeva eTMF
- Ensure compliance with regulatory and ethical standards
- Monitor trial progress and report findings
- Perform sponsor oversight activities within the Veeva eTMF and liaise between all stakeholders
- Coordinate sponsor activities and ensure alignment with trial objectives
INTERESTED? FOR THIS ROLE WE’RE LOOKING FOR THE FOLLOWING EDUCATION, EXPERIENCE, AND SKILLS:
- Bachelor’s degree or equivalent work experience in a clinical development work environment required
- 2+ years of experience in clinical research
- Strong organizational, communication and IT skills
- Knowledge of regulatory requirements and GCP guidelines
- Attention to detail and problem-solving skills
- Ability to work collaboratively in a team environment
- Proficiency with the Veeva Systems platform, especially Veeva eTMF
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
A clinical development work environment required
Proficient
1
Monheim, Germany
