Senior Global Regulatory Project Manager – Pharma

Syneos Health, Inc.; Viseu; On-site; EUR 85,000 - 120,000; Full time

Job summary

Syneos Health, Inc. invites an experienced Senior Regulatory Consultant to join our GRO RPSM portfolio.

You will provide global regulatory project management support to a dedicated sponsor and collaborate with Global Regulatory Affairs across regions, including Europe, the UK, and the Americas. Ideal candidates hold a life sciences degree (advanced degree preferred) and have 8+ years in regulatory affairs or project management, with proven experience in regulatory submissions and

Qualifications

• Bachelor's degree in life sciences; advanced degree preferred.
• Minimum of 8 years of experience in regulatory affairs or project management in pharma/biotech.
• Experience with global regulatory submissions and familiarity with FDA, EMA, ICH guidelines.
• Must have managed multiple Marketing Applications and/or LCM submissions across regions.

Responsibilities

• The Regulatory Project Manager role will work dedicated to a single Sponsor and provide regulatory project management support to the growing Sponsor Portfolio.

Skills

PM fundamentals

Communication

Organizational skills

Problem-solving

Timeline management

Risk management

Cross-functional collaboration

Education

Bachelor's degree in life sciences

Advanced degree preferred

Tools

Microsoft Office

Smartsheet

ThinkCell

Office Timeline

MS Project

Visio

Lucidchart

Veeva Vault RIM

Job description

Syneos Health, Inc. invites an experienced Senior Regulatory Consultant to join our GRO RPSM portfolio.

You will provide global regulatory project management support to a dedicated sponsor and collaborate with Global Regulatory Affairs across regions, including Europe, the UK, and the Americas. Ideal candidates hold a life sciences degree (advanced degree preferred) and have 8+ years in regulatory affairs or project management, with proven experience in regulatory submissions and