Pharmacovigilance Associate II/III - #1677612

Evestia Clinical


Date: 9 hours ago
City: Liverpool
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

How to apply

To apply for this job you need to authorize on our website. If you don't have an account yet, please register.

Post a resume

Similar jobs

M&E Client Side Project Manager- Data Centres

Eden Brown,
£500 - £650 / day
8 minutes ago
This is a Client side opportunity working within Construction Projects team for a significant Data Centre owner / operator on a Data Centre scheme about to start the pre con phase near Liverpool This is a busy role whereby you...
Eden Brown

Patient Advisor

Optical Express,
11 hours ago
Job Title: Patient Advisor Hours: Full Time 40 hours Location: Chiswick Salary: £27,000 + benefits Optical Express is focused on delivering exceptional patient care, outstanding clinical outcomes and continued investment in our people and technology. The Optical Express team work...

Copywriter

CONMED Corporation,
11 hours ago
CONMED is a global medical technology company that specializes in the development and manufacturing of surgical devices and equipment. With a mission to empower healthcare professionals to deliver exceptional patient care, CONMED is dedicated to innovation, quality, and excellence in...