Vizen Hiring PSUR/Signal Drafting, Peer Reviewer, Data Entry, Quality Reviewer

Pharmacovigilance Openings for Experienced Candidates

Vizen Lifesciences hiring experienced PV professionals for PSUR, Signal, QA, Data Review roles. Apply now.

Vizen Lifesciences is expanding its Pharmacovigilance operations and is looking for experienced PV professionals across multiple functional areas. These openings are ideal for candidates with hands-on exposure to safety data review, signal management, PSUR drafting, and quality oversight.

Company Overview

Vizen Lifesciences provides end-to-end drug safety and regulatory support to global pharmaceutical clients. The organization focuses on high‑quality pharmacovigilance services, compliance-driven processes, and timely safety reporting. With ongoing business expansion, the company is strengthening its PV teams with skilled safety professionals.

Job Role & Responsibilities

PSUR / Signal Drafting

Experience: Pharmacovigilance experience mandatory

Responsibilities:

• Prepare PSUR documents as per regulatory timelines.
• Support signal detection, evaluation, and documentation.
• Coordinate with safety physicians and review teams.
• Maintain compliance with global safety reporting standards.

Peer Reviewer

Experience: Pharmacovigilance experience mandatory

Responsibilities:

• Review case narratives, data accuracy, and safety outputs.
• Ensure completeness of ICSRs and related documentation.
• Identify gaps and provide corrective feedback.

Data Entry – PV

Experience: Pharmacovigilance experience mandatory

Responsibilities:

• Enter ICSR data into safety databases.
• Verify coding accuracy (MedDRA, WHO‑Drug).
• Maintain real‑time documentation and audit readiness.

Quality Reviewer

Experience: Pharmacovigilance experience mandatory

Responsibilities:

• Perform quality checks on safety case processing.
• Review compliance metrics and audit findings.
• Ensure adherence to SOPs, regulatory guidance, and internal quality parameters.

Eligibility / Qualifications

• Mandatory experience in Pharmacovigilance operations.
• Strong understanding of ICSR processing, MedDRA coding, and safety database workflows.
• Good communication, attention to detail, and quality‑focused mindset.

Location & Salary

Location will be shared directly by the company. Salary will be based on experience and role level.

Application Process

Interested candidates can apply by sending their updated resume to:
careers@vizenlifesciences.com

FAQs

Is pharmacovigilance experience mandatory?

Yes. These roles are only for candidates with prior PV experience.

Are freshers eligible?

No. Only experienced PV professionals should apply.

What profiles are open?

PSUR drafting, Signal management, Peer Review, Data Entry, and Quality Review.

What skills are required?

Strong knowledge of ICSR processing, safety reporting standards, MedDRA coding, and PV documentation.

Summary Table

Company	Vizen Lifesciences
Vacancies	PSUR/Signal Drafting, Peer Reviewer, Data Entry, Quality Reviewer
Required Education	Life sciences background with PV experience
Experience	PV experience mandatory