Medical Writing Lead
at Sanofi US
Budapest, Közép-Magyarország, Hungary -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Jan, 2025 | Not Specified | 20 Oct, 2024 | N/A | Management Skills,Regulations,Accountability,Conflict,English,Corporate Structure,Cultural Sensitivity,Delegation,Soft Skills,Regulatory Affairs,Drug Development,Teams,Regulatory Requirements,Languages,Leadership | 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:
SOFT SKILLS:
- Strong management skills including leadership, prioritization, team inspiration, cross-cultural sensitivity, delegation, empowerment, and accountability coupled with strategic and innovative thinking.
- Proven ability to manage changes, negotiate and influence others, and resolve conflict.
- Understanding of business considerations (basic finance, human resources).
- Ability to adapt to needs of an evolving business environment (e.g., regulatory requirements, corporate structure and processes, customer focus, technological advances).
- Ability to work across time zones and cultures.
Education:
- At least a bachelor’s degree, or equivalent, in regulatory affairs, the sciences, or related areas of study, and relevant experience.
Languages:
- Fluency in English, oral and written.
Responsibilities:
- Oversee the Medical Writing and Innovation Project Assistant employees and activities, with commitment to delivering high quality results and overcoming challenges with successful execution.
- Act as liaison to global functional leads on business topics such as metrics, prioritization, and performance.
- Foster employee development to build subject matter expertise and encourage collaboration with global functions to enhance knowledge sharing and drive process improvements.
- Promote teamwork, quality, operational efficiency, and innovation.
- Stay updated on evolving medical writing practices, regulatory and inspection readiness requirements to maintain industry leadership.
- Foster a change-agile environment and act as key change agent for new processes and technologies.
- Manage budgets and oversee initiatives to support legal requests, mergers, audits, inspections, and other organizational needs.
- Provide mentorship to staff, manage hiring and training processes, and ensure performance goals are met effectively.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Regulatory affairs the sciences or related areas of study and relevant experience
Proficient
1
Budapest, Hungary