Clinical Documentation and Quality Lead
at Sanofi US
Budapest, Közép-Magyarország, Hungary -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Nov, 2024 | Not Specified | 31 Aug, 2024 | N/A | Drug Development,Management Skills,Languages,Soft Skills,Leadership,Accountability,Cultural Sensitivity,Corporate Structure,English,Conflict,Regulatory Requirements,Diplomacy,Powerpoint,Delegation,Teams,Life Sciences | 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 title: Clinical Documentation and Quality Lead, R&D Hub Budapest
- Location: Budapest
- Flexible working: 60% home, 40% office
- Job type: Permanent, Full-time
TECHNICAL SKILLS:
- Good knowledge of MS Office Suite (Word, Excel, PowerPoint)
- Knowledge of electronic document management systems and resource planning
Education: At least a bachelor’s degree, or equivalent, in life sciences, or related areas of study, and relevant experience.
Languages: Fluency in English (written and spoken).
Responsibilities:
- Lead the Hub Clinical Documentation and Quality activities, with commitment to delivering high quality results and overcoming challenges with successful execution.
- Act as liaison to global functional heads on business topics such as metrics, prioritization, and performance.
- Develop team leaders and employees to enhance skills and promote collaboration across functions, optimizing resource allocation.
- Implement technology and process improvements to streamline document preparation and reduce costs effectively.
- Stay updated on evolving medical writing practices, regulatory and inspection readiness requirements to maintain industry leadership.
- Manage budgets and oversee initiatives to support legal requests, mergers, audits, inspections, and other organizational needs.
- Provide mentorship to staff, managing hiring and training processes, and ensuring performance goals are met effectively.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Life sciences or related areas of study and relevant experience
Proficient
1
Budapest, Hungary