Pharmacovigilance Associate (Hybrid)

Society for Conservation Biology; Rahway (NJ); Hybrid; USD 70,000 - 90,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a detail-oriented Pharmacovigilance Associate. The ideal candidate will have a background in veterinary technology or life sciences. This hybrid role requires strong communication and organizational skills, as well as proficiency in Microsoft Office. Join a team dedicated to ensuring safety in pharmaceuticals while working in a collaborative environment.

Qualifications

• Degree in veterinary technology, life sciences, or equivalent experience.
• Strong communication, organizational, and collaboration skills.
• Experience in a veterinary clinic or pharmacovigilance preferred.

Responsibilities

• Review, approve, and submit individual case safety reports.
• Support aggregate adverse event report preparation.
• Track PV team metrics and assist with PV projects.

Skills

Communication

Organizational

Collaboration

Education

Degree in veterinary technology

Degree in life sciences

Tools

Microsoft Office

Job description

Employer: Freyr Solutions
Client: Global Pharma company
Location: Rahway, New Jersey, US
Salary: Competitive
Closing date: May 14, 2025

Sector:

Consultancy/Private Sector

Field:

Conservation science

Discipline:

Biology

Salary Type:

Salary

Employment Type:

Full time

Position:

Pharmacovigilance Associate (Hybrid - 3 Days Onsite)

Location:

Rahway, NJ

Schedule:

Hybrid - Required onsite Tuesday & Wednesday + Monday or Thursday. Remote on Friday.

Job Description:

We are seeking a detail-oriented Pharmacovigilance Associate to join our team. Ideal candidates will have a background in veterinary technology, life sciences, or pharmaceutical industry experience.

Qualifications:

• Degree in veterinary technology, life sciences, or equivalent industry experience
• Strong communication, organizational, and collaboration skills
• Proficiency with Microsoft Office (Outlook, Excel, PowerPoint)
• Preferred: Experience in a veterinary clinic, pharmacovigilance, or highly regulated pharmaceutical environment

Responsibilities:

• Review, approve, and submit individual case safety reports
• Support aggregate adverse event report preparation
• Archive PV documents and support administrative activities
• Track PV team metrics and assist with PV projects as needed