safetymid

Pharmacovigilance Specialist

Detects, processes and reports adverse events across a product's life.

Also known as: PV Specialist · Drug Safety Associate · DSA

Get the role brief Train for this role
Salary band (US)
$80k–$135k
Salary band (UK)
£40k–£80k
Typical YoE
2–6 years; medical background common

What the role is

PV professionals receive case reports from trials and post-market sources, code them with MedDRA, assess seriousness and expectedness, and submit ICSRs to regulators within the required windows. PSUR/PBRER aggregate authoring is the senior end of the function.

A typical day

  • Triage 25 incoming AE reports for seriousness
  • MedDRA coding session with the medical reviewer
  • Argus case narrative QC
  • Draft a 7-day SUSAR submission
  • Aggregate report data pull for an upcoming PBRER

Required skills

MedDRA codingArgus / ARISgICH E2A/E2B/E2DCausality assessmentAggregate report authoring

Certifications that matter

Career ladder

Junior
PV Associate
This role
PV Specialist
Next
Senior PV → PV Manager → QPPV (EU)

Request the Pharmacovigilance Specialist role brief

Request the Pharmacovigilance Specialist brief

Salary benchmarks, scorecard, and 3 verified candidates — sent within one business day.

No spam. We reply within one business day.

Hiring a Pharmacovigilance Specialist?

We can place a verified candidate in 2 weeks, with the dossier you actually need to make the call.

Request a brief Train one instead
All career paths