Pharmacovigilance Consultant
Part time (2/4 days)
3 month contract
Competitive salary - can be discussed upon application
Can be fully Remote
Are you seeking new opportunities? We have an excellent role for you if you're looking to move away from full-time work in a large company
We are seeking a passionate Pharmacovigilance professional with multiple years of experience to work 2-3 days with our small, dedicated company. This role offers numerous opportunities to contribute to our mission of enhancing patients' lives.
You will serve as the primary contact for pharmacovigilance and provide medical information support for the business as needed.
Key Responsibilities
- Manage PV contracts end-to-end, including SDEAs/PVA/TAs.
- Review Technical Agreements as needed.
- Oversee daily management and monitoring of two PV mailboxes.
- Interact with health authorities for PV as needed.
- Maintain strong relationships with internal departments and international partners.
- Support the UK/EU QPPV and PV teams in maintaining the pharmacovigilance system.
Qualifications
- Minimum of 5 years' experience in a PV environment, including PV audits and inspections.
- Degree educated, preferably in Life Sciences.
- Extensive knowledge of UK and EU PV regulatory requirements (e.g., GPvP and GVP) related to drug safety, with a solid understanding of methodologies for compliance in signal detection and evaluation, risk/benefit assessments, and implementation of pharmacovigilance risk minimization strategies.
- Proficient in Microsoft applications.
- Highly motivated with the ability to understand technical content and communicate it clearly and concisely.
- Proven success in self-managing priorities and handling multiple projects simultaneously
If you do not hear back from Projectus Consulting within 7 days, please assume that your application has not been proceeding on this occasion only.