puestos de Clinical Research en United States

Direct message the job poster from 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 sarah@fusiongroupglobal.com

• Seniority level
  Associate

• Employment type
  Full-time

• Job function
  Project Management, Administrative, and Quality Assurance
• Industries
  Biotechnology Research and Pharmaceutical Manufacturing

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