Experienced Clinical Safety Coordinator
at Medpace Inc
80339 München, Bayern, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 26 May, 2024 | Not Specified | 01 Mar, 2024 | N/A | Turkish,English,Medical Terminology | 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:
Job Summary :
Our Turkish activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team, in Germany! This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities :
- Responsible for the distribution of safety reports to regulatory authorities;
- Create and maintain project-related trackers and status reports;
- Distribute and track safety-related notifications;
- Conduct quality control reviews of departmental documents;
- Regular interaction with other internal departments globally and locally, such as, Clinical Operations, Data Management and Regulatory Submissions;
- Perform other tasks as needed.
Qualifications :
- Educated to degree level, Bachelor of Science
- Strong attention to detail
- Comprehensive understanding of Microsoft office suite
- Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology (preferred, not mandatory)
- Knowledge of Electronic Data Capture (EDC) systems and other clinical databases (preferred, not mandatory)
- Knowledge of applicable safety reporting guidelines (preferred, not mandatory)
- Fluency in English and Turkish is required.
Responsibilities:
- Responsible for the distribution of safety reports to regulatory authorities;
- Create and maintain project-related trackers and status reports;
- Distribute and track safety-related notifications;
- Conduct quality control reviews of departmental documents;
- Regular interaction with other internal departments globally and locally, such as, Clinical Operations, Data Management and Regulatory Submissions;
- Perform other tasks as needed
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
80339 München, Germany