Senior Pharmacovigilance Consultant
Be part of our award-winning team South Oxfordshire, UK Part time is an option Permanent contract, competitive salary plus benefits Not your average PV role
- Are you looking to diversify your role and have a fuller appreciation of the drug development and life-cycle process?
- Are you looking to work in a smaller company environment with increased visibility?
- Are you looking for a more flexible working environment/work-life balance?
Use your PV knowledge across a broad spectrum of projects integrating closely with the regulatory team on MAAs, CTAs and writing of safety documents. EUDRAC is an expanding regulatory and pharmacovigilance consultancy company and we are now looking to recruit a Senior Pharmacovigilance Consultant to our UK office based in a countryside setting 10 minutes from the M40 (J6 and 7) and 15 minutes from Oxford.
EUDRAC provides regulatory and pharmacovigilance support to drive products through clinical development, registration and life-cycle support in the EU countries.
Our clients range from large multinational companies to small start-ups in Europe and USA.
We need someone with:
- Good initiative
- Attention to detail
To find out more about this exciting role, please contact Carole Pugh, Managing Director, EUDRAC Ltd at email@example.com. STRICTLY NO AGENCIES See the job description at www.eudrac.com/about-eudrac