Job Advert
We are looking for a well organised and solution based 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 383886 Email: mkeiller@nhs.net
Internal candidates must have written approval from their line manager prior to applying for this as a secondment. You will be required to bring this if shortlisted for interview. The successful applicant will return to a post within their substantive department at their substantive grade at the end of the secondment period.
Hours of work are: 37.5 hours per week
NHS Tayside is committed to equality and diversity and welcomes applicants from all sections of the community.
Short-listed applicants will be contacted by email. Please check your emails regularly, including your junk/spam folder.