IQVIA Hiring Pharmacovigilance Specialist 2

Pharmacovigilance Specialist 2 – Life Sciences Graduate | Bengaluru

IQVIA hiring Pharmacovigilance Specialist 2 in Bengaluru. Min 3 years clinical safety experience. Hybrid role. Apply online.

Begin a high-impact safety career with IQVIA as a Pharmacovigilance Specialist 2 in Bengaluru. This role is ideal for professionals with strong case-processing experience, solid understanding of ICH-GCP, and the ability to lead moderate to complex clinical safety programs.

---

Company Overview

IQVIA is a global leader in advanced analytics, clinical research, and technology-enabled healthcare services. With operations in over 100 countries, the company supports biopharma, medical device, and CRO-driven innovation through data-driven safety operations, clinical research execution, and regulatory compliance. Working with IQVIA means contributing to patient safety worldwide while developing your expertise through continuous learning and leadership exposure.

---

Job Role & Responsibilities

The Pharmacovigilance Specialist 2 supports complex safety programs and performs end-to-end case processing while also operating as a Safety Management Lead on larger studies.

Core Responsibilities

• Perform comprehensive case-processing tasks including intake, triage, data entry, narrative writing, QC, reconciliation, and regulatory reporting.
• Lead safety management activities for moderate–large studies with minimal supervision.
• Develop study-specific safety documents such as Safety Management Plans and SAE forms.
• Attend client meetings, investigator meetings, and provide internal training on safety processes.
• Ensure compliance with budget, timelines, and project scope.
• Mentor junior safety associates and support team-level performance.
• Escalate critical safety issues appropriately and ensure inspection readiness.
• Assist in bid defenses, client presentations, and operational planning when required.

---

Eligibility / Qualifications

Education

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related healthcare field.

Experience

• Minimum 3 years of clinical trial safety experience.
• Hands-on experience in case processing, narrative writing, and regulatory reporting.
• Strong understanding of pharmacovigilance regulations, ICH-GCP, and safety data handling.

Skills & Competencies

• Excellent written and verbal communication.
• Ability to analyze safety data and resolve discrepancies.
• Experience with EDC systems and electronic safety databases.
• Strong organizational and multitasking abilities.
• Ability to guide, mentor, and support team members.
• Independent problem-solving with minimal oversight.

Relevant Courses (comma-separated)

B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Clinical Research, PV Certification, Drug Safety Training, Pharmacovigilance Diploma.

---

Location & Salary

• Location: Bengaluru
• Work Model: Hybrid
• Employment: Full-time
• Compensation: Competitive and aligned with PV industry standards

---

Application Process

Submit your application through the official IQVIA careers portal:
👉 Apply Here: https://jobs.iqvia.com/en/job/-/-/24443/88677835696

---

FAQs

1. What is the minimum experience required?

At least 3 years of clinical safety or pharmacovigilance experience.

2. Is team leadership required?

Yes. You will mentor junior staff and may lead safety activities on complex studies.

3. Does this role involve case processing?

Yes. End-to-end ICSR processing is a key responsibility.

4. Is this a hybrid role?

Yes. The position follows IQVIA’s hybrid working model.

5. Who should apply?

Candidates with strong PV expertise, ICH-GCP understanding, and leadership capability.

---

Summary Table

Company	IQVIA
Vacancies	Pharmacovigilance Specialist 2
Required Education	Bachelor’s in Life Sciences/Pharmacy/Healthcare
Experience	Minimum 3 years in clinical trial safety

---

Grow your pharmacovigilance career by contributing to global safety programs with IQVIA’s experienced safety operations team.