SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.
The Role
Ensure the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams.
Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic region.
My client, a prominent player in the healthcare industry, is renowned for developing groundbreaking products in diagnostics, medical devices, nutrition, and branded generic pharmaceuticals.
Contract Duration: 12 months initially, potential for permanent work afterwards
With a global workforce of 114,000 employees spread across more than 160 countries, they are committed to making a lasting impact on health.
AbbVie is a global biopharmaceutical company with focus and capabilities to address some of the world's greatest health challenges, combining advanced science, expertise, and passion to solve serious health issues and have a remarkable impact on people's lives.
Are you ready to take the lead in securing critical business contracts?
We're seeking a proactive and detail-oriented Contract Specialist to join our dynamic team at our Maidenhead office.
In this role, you'll play a pivotal part in our tender submission process, working closely with Contracts Managers across the country to deliver accurate and timely bids.