Pharmacovigilance Associate II/III

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

Job summary

Join a forward-thinking company as a Pharmacovigilance Associate II, where you'll lead case management activities and ensure compliance in drug safety. This role is perfect for those who thrive in a collaborative environment and are passionate about making a real impact in healthcare. You'll mentor junior team members, liaise with clients, and contribute to regulatory deliverables. With opportunities for career development and a commitment to improving patient safety, this position offers a rewarding path in the biotechnology sector. Embrace the chance to grow in a dynamic team dedicated to innovation and excellence.

Benefits

Career Development Opportunities

Collaborative Work Environment

Flexible Working Hours

Qualifications

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

Responsibilities

• Lead case management activities including triage and follow-up.
• Ensure timely reporting of safety data to regulatory authorities.

Skills

Pharmacovigilance

Case Management

Regulatory Compliance

Attention to Detail

Organizational Skills

Education

Degree in Pharmacy

Degree in Biological Sciences

Tools

eVigi

eSafety

Veeva

Job description

Direct message the job poster from Evestia Clinical

Specialist Life Science Recruiter & Talent Partner

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 [e-mail]

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management, Administrative, and Quality Assurance

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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