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Are you an experienced physician in clinical research? Are you keen to use your skills and clinical knowledge to work towards further advancements in medicines and continue work on life changing treatments? If this sounds like something you are looking for then we have the role for you!
Compass Life Sciences are delighted to be working in partnership with a leading UK based CRO in their search for a Clinical Safety Research Physician. Due to ongoing business wins with an extensive portfolio of studies our client is looking to expand on their team with this appointment.
In this role you will be contributing to the development of trial specific safety reporting and trial documents such as protocols study operations manuals and pharmacovigilance plans as well as contributing to core safety information. You will also be medically responsible for reporting to relevant appointments, such as sponsors and authorities, any adverse events and adverse drug effects that may occur during clinical trials and responsibility for any tracking and follow ups required.
This is a role that will involve working with a number of cross functional teams including Pharmacovigilance teams, Medical teams and Clinical teams, to provide input into any case reporting, development of efficient PV in the business and mentor more junior members of the team. You will also work with external teams and over view of any incoming drug safety reports.
For this role the ideal candidate will possess the following
In exchange our client is offering a competitive salary with a great benefits package and progression opportunities.
Compass Associates Ltd. trading as Compass Life Sciences are acting as a Recruitment Consultancy for this permanent vacancy; we offer £200 worth of John Lewis Vouchers for each successful recommendation.