Search

Pharmacovigilance Associate II/III

Evestia Clinical
locationUnited Kingdom
PublishedPublished: Published today
Full Time

Job Title: PVG Associate II/ III

Location: Remote in the UK

Department: Clinical Development Division


At Evestia Clinical, we’re on a mission to support innovation in healthcare, and we’re looking for a Pharmacovigilance (PVG) Associate II to join our dynamic Case Management Team. If you thrive in a collaborative, fast-paced environment and are passionate about drug safety and compliance, this could be the perfect next step in your PVG career.


What will the role entail?

  • Lead and support day-to-day case management activities including case triage, processing, tracking, and follow-up.
  • Liaise with clients and internal teams on project updates, timelines, and deliverables.
  • Mentor and support junior team members to ensure accuracy, quality, and compliance across all PVG tasks.
  • Assist with developing and reviewing SOPs and working instructions for pharmacovigilance systems.
  • Collaborate with project leaders on regulatory deliverables (e.g., PSURs, RMPs, PSMFs).
  • Ensure accurate and timely reporting of safety data to regulatory authorities, clients, and stakeholders.
  • Support audit and inspection readiness, and participate in audits when required.
  • Contribute to continuous improvement of internal processes and support fee invoice generation when needed.
  • Manage the Drug Safety mailbox and case intake.
  • Use PV systems (e.g., eVigi, eSafety, Veeva) to ensure compliance and tracking.
  • Support reconciliation, follow-up schedules, MedDRA coding, and narrative preparation.
  • Provide backup support to PV Assistants and Leads when needed.
  • Attend client meetings and collaborate cross-functionally.


What will you need to succeed?

  • A degree in Pharmacy, Biological Sciences, or related field.
  • Previous experience in pharmacovigilance is a necessity.
  • Experience in both case management and submissions is advantageous.
  • Previous experience in a CRO or with biotech clients is a plus.
  • Excellent attention to detail, organizational skills, and ability to work to strict deadlines.


Why Join Us?

  • Be part of a growing team dedicated to improving patient safety worldwide.
  • Work in a collaborative, flexible environment with career development opportunities.
  • Make a real impact in projects that matter.


Interested?

Apply to the role below or email the recruiter sarah@fusiongroupglobal.com