Pharmacovigilance Associate II/III - #1677709

Evestia Clinical


Date: 11 hours ago
City: Cardiff
Contract type: Full time
Work schedule: Full day
Evestia Clinical

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 *****@fusiongroupglobal.com

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