Senior Pharmacovigilance Scientist
I am currently working with a top pharmaceutical company in Hertfordshire who is looking for a Senior Pharmacovigilance Scientist to join their PV team for a 12-month contract. The company is looking for someone who will be accountable for workload monitoring and balancing resource for the Data Governance and Standard team in collaboration with other PV teams.
Some of your responsibilities will be:
*Assist in providing data for ICSR Governance
*Oversight of ICSR submission to EudraVigilance
*Keeping up to date with European legislation and guidelines
*Address and improve submission compliance
*Participate in the prioritisation, review and delivery of Discrete ICSR Package Projects within agreed timelines
*Monitoring, reviewing, trouble-shooting and tracking status
*Review of database searches
*Developing tactical solutions to investigate and address case processing inconsistency and ARISg system issues
*Represent the department at internal and external forums
*Assist with Inspection Readiness
The company is looking for someone who has drug safety/pharmacovigilance experience working in a pharmaceutical company, knowledge of global PV regulatory obligations with the ability to evaluate, analyse and interpret data.
If you are interested in discussing this role further, please get in touch with Sabrina Deo at firstname.lastname@example.org or 0121 616 3471
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Job Reference: Sd-SrPvscientist_1532342130
Broadcast As: 204
Salary To: Negotiable
Job Type: Full Time
Job Term: Contract
Job Industry: Pharmaceutical
Job Specialism: Pharmacovigilance
Recruitment Consultant: Sabrina Deo