Global Regulatory Ops Director & Veeva RIM SME

Pacira BioSciences, Inc.; Parsippany-Troy Hills (NJ); Vor Ort; USD 141.000 - 194.000; Vollzeit

Benefits dieser Stelle

Medical, Prescription, Dental, Vision

401(k) with company match

Flexible Time Off & 11 paid holidays

Parental Leave

Life insurance

Employee Assistance Program

Zusammenfassung

Pacira BioSciences, Inc. is seeking an Associate Director of Regulatory Operations to drive global regulatory strategy and lead submission planning across regions. The role focuses on optimizing processes, ensuring timelines, and leveraging Veeva RIM as a SME to enhance efficiency and compliance.

The candidate will oversee cross‑functional collaboration, data governance, and lifecycle management while delivering training and process improvements across the regulatory organization.

Qualifikationen

• Bachelor’s degree in life sciences or related field.
• 8+ years of experience in Regulatory Operations within pharma/biotech.
• Deep hands‑on expertise with Veeva RIM functionalities and workflows.
• Experience with global regulatory submission planning, tracking, and lifecycle management.

Aufgaben

• Develop and maintain integrated regulatory plans aligned with global development strategies.
• Provide portfolio-level visibility and reporting on submission progress and risks.
• Lead end‑to‑end submission planning and tracking within Veeva RIM.
• Ensure compliance with global regulatory requirements and timelines.
• Partner with Regulatory Affairs leads to translate strategies into operational plans within Veeva.

Kenntnisse

Regulatory submissions planning

Multi-region submissions

Regulatory governance

Veeva RIM

Cross-functional projects

Training delivery

Data analysis

Ausbildung

Bachelor’s degree in life sciences or related field

Tools

Veeva RIM

Jobbeschreibung

Pacira BioSciences, Inc. is seeking an Associate Director of Regulatory Operations to drive global regulatory strategy and lead submission planning across regions. The role focuses on optimizing processes, ensuring timelines, and leveraging Veeva RIM as a SME to enhance efficiency and compliance.

The candidate will oversee cross‑functional collaboration, data governance, and lifecycle management while delivering training and process improvements across the regulatory organization.