Pharmacovigilance Safety Surveillance Specialist

Venesco,-LLC-

Frederick (MD)

On-site

USD 70,000 - 100,000

Full time

14 days+
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Job summary

Venesco LLC is seeking a Safety Surveillance Support Specialist to support pharmacovigilance and clinical safety activities by processing safety reports, monitoring adverse event information, maintaining safety databases, and supporting regulatory reporting requirements.

Duties include monitoring safety email inboxes, receiving and triaging adverse event reports, processing safety cases, supporting MedWatch submissions, reconciling safety databases, and preparing inspection-ready documentation.

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Public Health, or related field.
  • Minimum 3 years of pharmacovigilance or drug safety experience.
  • Familiarity with Argus or similar safety systems.
  • Knowledge of FDA and ICH safety reporting requirements.

Responsibilities

  • Monitor safety email inboxes and reporting systems.
  • Receive and triage adverse event reports.
  • Process safety cases and follow-up information.
  • Support MedWatch and regulatory reporting submissions.
  • Reconcile clinical and safety databases.
  • Maintain safety documentation and records.
  • Support DSMB preparation and logistics.
  • Assist with safety trend analysis.
  • Support annual safety reports and study closeout activities.

Skills

Pharmacovigilance
Safety reporting
Regulatory compliance

Education

Bachelor's degree in Life Sciences, Nursing, Public Health, or related field

Tools

Argus

Job description

Venesco LLC is seeking a Safety Surveillance Support Specialist to support pharmacovigilance and clinical safety activities by processing safety reports, monitoring adverse event information, maintaining safety databases, and supporting regulatory reporting requirements.

Duties include monitoring safety email inboxes, receiving and triaging adverse event reports, processing safety cases, supporting MedWatch submissions, reconciling safety databases, and preparing inspection-ready documentation.

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