Medical Writing Lead

at  Sanofi US

Budapest, Közép-Magyarország, Hungary -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Jan, 2025Not Specified20 Oct, 2024N/AManagement Skills,Regulations,Accountability,Conflict,English,Corporate Structure,Cultural Sensitivity,Delegation,Soft Skills,Regulatory Affairs,Drug Development,Teams,Regulatory Requirements,Languages,LeadershipNoNo
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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