Job Advert
NHS Scotland is committed to encouraging equality and diversity among our workforce and eliminating unlawful discrimination. The aim is for our workforce to be truly representative and for each employee to feel respected and able to give their best. To this end, NHS Scotland welcomes applications from all sections of society.
We are looking for an individual to deliver Pharmacovigilance and safety reporting for the portfolio of clinical research trials sponsored by NHS Tayside/University of Dundee.
The successful candidate will have a first degree in a relevant discipline with experience in research/clinical research or audit. You will have well developed written and verbal communication skills, including the ability to interpret and communicate complex information, along with first rate numeracy and IT/data management skills.
You will have knowledge of the clinical trials regulatory environment, excellent interpersonal and relationship management skills with proven report writing ability. A track record demonstrating accuracy and attention to detail is essential. Evidence of further education including postgraduate degree and experience of working within the NHS, University environment or Pharmaceutical Industry/Clinical Research Organisation would be an advantage.
Informal enquiries to Marney Keiller, Senior Clinical Trials Monitor Tel: 01382 660111 ext 59028 Email: Marney.Keiller@nhs.scot
You will be employed by NHS Tayside. Hours of work are: 37.5 hours per week
Fixed Term/ Secondment for 12 months
Internal candidates: *Written approval must be sought from your line manager prior to applying for this secondment. You will be required to bring this if shortlisted for interview.
Shortlisted applicants will be contacted by email. Please check your emails regularly, including your junk/spam folder.