An established industry player is seeking an experienced Business Analyst with a strong background in regulatory affairs and GxP processes. This role requires a detail-oriented professional who can thrive in a fast-paced, team-oriented environment. The ideal candidate will have over 8 years of experience in business analysis, particularly within pharmaceutical R&D life sciences. You will be responsible for managing submission content and navigating the complexities of global regulatory affairs. If you are passionate about making a difference in the life sciences sector and have the skills to tackle challenges proactively, this is an exciting opportunity for you.
Qualifications
8+ years of experience as a Business Analyst required.
Knowledge of Pharmaceutical R&D Life Sciences is essential.
Responsibilities
Work independently and collaboratively in a fast-paced environment.
Raise challenges early and develop mitigation strategies.
Skills
Business Analysis
Regulatory Affairs
GxP Processes
Communication Skills
Detail Oriented
Tools
Generis CARA
Job description
Mandatory Skills - Business Analyst with Regulatory experience; GxP process experience required
8+ years of experience as BA
Working knowledge of Pharmaceutical R&D Life Sciences
Specific knowledge of Global Regulatory Affairs, submission content management and publishing, and Generis CARA product preferred
Knowledge of GxP processes is required for the role
Ability to work independently and with team
Detail oriented and strong communication skills
Ability to raise challenges/ concerns early and develop mitigation strategies to address
Comfortable working in a fast-paced, team-based environment