I am working with a top pharmaceutical company in Hertfordshire who is recruiting for a Drug Safety Specialist to join them on a 6-month contract and this role can be full-time or part-time. This role will be overseeing the ICSR processes and PV systems.
The team use their pharmacovigilance expertise, particularly individual case safety report (ICSR) knowledge, to ensure safety data is processed and reported in a high quality, compliant manner, so it can be used to understand and communicate the product benefit risk to protect patients' safety.
Some of your responsibilities include; maintaining procedural documents and training, devises strategies and solutions to contain issues, mitigate risks and develop solutions, is transparent with risks identified and escalates to BPO/GPO network where necessary.
The company is looking for someone who has:
*Profound knowledge of assigned topics and regulations within ICSR case processing, & strong broad knowledge across the end to end ICSR process in line with the expectations of the key stakeholders
*Pharmacovigilance experience working in the industry
*Good knowledge of international regulations (ICH, EU GVP Modules, FDA) and an understanding of the pharmaceutical industry (product development and the commercial environment
If you would be interested in discussing this role then please get in touch with Sabrina Deo at firstname.lastname@example.org
You must be eligible to work in the UK. Learn more
- Agency: Paramount Recruitment
- Reference: sd-ICSR
Website: Paramount Recruitment
- Posted: 19th February 2021
- Expires: 5th March 2021