Regulatory Compliance Specialist

hace 2 semanas


Madrid, Madrid, España Tbwa ChiatDay Inc A tiempo completo

Job Description:
Tbwa Chiat/Day Inc is seeking a highly skilled Regulatory Manager to join our team. As a key member of the Precision for Medicine team, you will play a crucial role in providing regulatory strategy and development guidance for clinical trials.

Key Responsibilities:
- Provides regulatory guidance throughout the clinical development life cycle
- Coordinates and prepares regulatory documents for submission to Regulatory Authorities and/or Ethics Committees
- Develops and reviews documents intended for submission to Regulatory Authorities and/or Ethics Committees to ensure compliance with regulatory standards
- Represents Global Regulatory Affairs at project team meetings with both external and internal customers
- Oversees and coordinates Regulatory Affairs Specialists to achieve submission targets for contracted programs

Essential Skills and Qualifications:
- Bachelor's degree in a relevant field (e.g., law, medicine, science)
- Proven experience in regulatory affairs, preferably in the pharmaceutical or biotechnology industry
- Excellent analytical, communication, and problem-solving skills
- Ability to work effectively in a team environment and lead projects as required

Salary and Benefits:
The salary range for this position is approximately $120,000 - $160,000 per year, depending on qualifications and experience. Additional benefits include health insurance, retirement savings plan, and paid time off.



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