An exciting opportunity has arisen at the Centre for Trials Research (CTR) for two specialists in pharmacovigilance and safety to ensure the accurate entry, coding and reporting of all pharmacovigilance and safety data, and to provide support and advice to the trial teams on the pharmacovigilance and safety requirements dictated by the Clinical Trials Regulations.
The CTR is the largest group of academic clinical trials staff in Wales, and has earned full UK Clinical Research Collaboration (UKCRC) registered status. The Centre tackles the big diseases and health concerns of our time, including growing resistance to antibiotics, early cancer diagnosis and how to eliminate health inequalities. It achieves this by forming partnerships with researchers and building lasting relationships with the public, whose participation is essential for the success of studies.
You should have a degree/NVQ 4 or equivalent professional membership/experience and substantial experience of working within pharmacovigilance and safety.
Salary: £27,025 to £31,302 per annum
Hours: Full time, part time
Contract type: Permanent, fixed-term/contract
Job reference: 8349BR
Closing date: 1 April 2019