Junior Pharmacovigilance Advisor
We have an opening for a Junior Pharmacovigilance Advisor within our well established team. A full-time position with the option of working to a hybrid working model, if required.
PURPOSE / KEY RESPONSIBILITIES:
- Adherence to the Acorn Quality System and Pharmacovigilance Quality System.
- Responsible for drafting PVAs and SDEAs and driving them to finalization with all clients and business partners. including on-going maintenance and updates of PVAs / SDEAs when required.
- Track and ensure timely completion of periodic reconciliations with client and business partners.
- Engages in quality system continuous improvement initiatives to enforce the quality culture.
- Assist with GVP inspection readiness activities.
- Assist in the investigation of non-conformances and CAPA management.
- Assist team with Pharmacovigilance compliance activities, KPIs, and metric management.
- Support the company during client audits and authority inspections.
- Screening of Local and Global Literature for Safety information when required.
Knowledge and Skills
- B.Sc. in Pharmacy or Science related discipline as minimum.
- Experience working within a pharmacovigilance or quality systems environment involving the research, interpretation and application of legislation.
- Awareness and understanding of Pharmacovigilance legislation in Europe and the UK.
- Know-how of pharmacovigilance and quality management systems and procedures.
- Commercial awareness & an innate ability to assess the commercial implications of decisions and advice.
- Good project management skills with a systematic approach to tasks.
- Ability to keep meticulous records and attention to detail.
- Above average communication skills both written and oral, with the ability to influence.
- Motivated self-starter with the ability to work independently.
- Confidence to embrace new challenges within the parameters of qualifications and experience.
To apply for this job email your details to info@acornregulatory.com.