Regulatory Affairs Consultant - Switzerland & Germany
at Parexel
Home Office, Georgia, Switzerland -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 18 Dec, 2024 | Not Specified | 20 Sep, 2024 | N/A | Good communication skills | 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:
Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team!
Responsibilities:
- Provide strategic guidance on regulatory requirements and submissions in Germany and Switzerland
- Support national dossier filings and contribute to centralized dossier preparation
- Offer expert advice on new product applications and lifecycle maintenance
- Lead small-scale projects or work streams, ensuring client satisfaction and project success
- Collaborate with cross-functional teams to deliver high-quality regulatory solutions
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
A scientific area
Proficient
1
Home Office, Switzerland
