Cencora PharmaLex is looking for an experienced Senior Trial Master File Study Owner to work within our Professional Services team on a full-time, 6 month fixed-term contract.
Are you a Trial Master File expert looking for your next role?
Then, Cencora Pharmalex is your career opportunity!
Research has been happening across the National Trust for over a century, and is key to helping us look after and bring to life the special places in our care.
We now have an exciting opportunity to join two of the teams who help make this happen.
We're looking for a highly motivated person to join us as a Research Officer, to support both our Central & South West Research Teams.
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.
General
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.
FPSG are pleased to offer a number of contract opportunities for User Researchers at all levels for roles working on UK Based projects, with SC Clearance.
It is helpful if you already have SC Clearance, however, if you do not currently hold this, it can be obtained through the process if you meet the SC Clearable criteria.
If unsure, please get in touch and we can support you with your queries on this.