Pharmacovigilance Associate II/III

JR United Kingdom; United Kingdom; Remote; GBP 35,000 - 55,000; Full time

Job summary

Join a forward-thinking company dedicated to improving patient safety worldwide as a PVG Associate II/III. In this dynamic role, you will lead case management activities, mentor junior team members, and collaborate on regulatory deliverables. If you have a passion for drug safety and compliance and thrive in a collaborative environment, this position offers a unique opportunity to make a real impact in healthcare innovation. With a focus on continuous improvement and career development, you will be part of a growing team that values your contributions and supports your professional growth.

Benefits

Career Development Opportunities

Collaborative Work Environment

Flexible Working Hours

Qualifications

• Degree in Pharmacy or Biological Sciences required.
• Previous experience in pharmacovigilance is a necessity.

Responsibilities

• Lead day-to-day case management activities and ensure compliance.
• Liaise with clients and internal teams on project updates.

Skills

Pharmacovigilance

Case Management

Attention to Detail

Organizational Skills

Education

Degree in Pharmacy

Degree in Biological Sciences

Tools

eVigi

eSafety

Veeva

Job description

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Client:

Evestia Clinical

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

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.