Pharmacovigilance Specialist

Talent Groups; Waltham (MA); On-site; USD 82,656 - 86,788; Part time

Job summary

A leading recruitment firm is looking for a Senior Technical Recruiter specializing in Pharmacovigilance. This role will support safety surveillance and signal management across clinical and post-marketing products. Key responsibilities include performing safety data analysis and authoring safety documentation. The ideal candidate will have a life sciences degree and 2-4 years of pharmacovigilance experience. This is a contract position based in Waltham, Massachusetts, offering a competitive hourly rate between $60.00 and $63.00.

Qualifications

• 2–4 years of pharmacovigilance experience required.
• Experience with safety reporting is necessary.

Responsibilities

• Support product safety surveillance and signal detection activities.
• Contribute to risk management plans and benefit-risk assessments.
• Perform safety data analysis and author safety documentation.
• Provide PV input to clinical and regulatory documents.
• Collaborate with cross-functional and vendor partners.

Skills

Strong communication skills

Analytical skills

Organizational skills

Education

Life sciences or healthcare degree

Tools

MedDRA

Job description

Senior Technical Recruiter at Talent Group

The Pharmacovigilance Scientist will support safety surveillance and signal management activities across clinical and post-marketing products. This role partners closely with PV Physicians and cross-functional teams to manage risk, contribute to regulatory deliverables, and ensure compliance with global pharmacovigilance requirements.

Base pay range

$60.00/hr - $63.00/hr

Key Responsibilities

• Support product safety surveillance and signal detection activities
• Contribute to risk management plans (RMPs/REMS) and benefit-risk assessments
• Perform safety data analysis and author safety documentation
• Provide PV input to clinical and regulatory documents
• Collaborate with cross-functional and vendor partners

Qualifications

• Life sciences or healthcare degree
• 2–4 years of pharmacovigilance experience
• Experience with safety reporting and MedDRA
• Strong communication, analytical, and organizational skills

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Health Care Provider and Research
• Pharmaceutical Manufacturing and Biotechnology Research

Cambridge, MA