Associate Pharmacovigilance ICSR Openings for Life Sciences in Hyderabad
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Professional Expectations
- Eligibility / Qualifications
- Required Education
- Required Experience
- Preferred Qualifications
- Behavioral Competencies
- Location & Salary
- Application Process
- FAQs
- Who is eligible for this role?
- Is this a case-processing role?
- Does the job involve global collaboration?
- Which systems are preferred?
- What education background is required?
- Summary Table
Apply for Associate Pharmacovigilance ICSR roles in Hyderabad. Openings for Life Sciences, Pharmacy, Nursing graduates with 2–5 years experience.
Johnson & Johnson is hiring Associate Pharmacovigilance Specialists for its ICSR function in Hyderabad. This opportunity is ideal for safety professionals who understand case processing and want to work with global patient safety systems, digital innovation, and data‑driven pharmacovigilance operations. The role supports capability development, operational improvements, and system enhancements across global case management.
Company Overview
Johnson & Johnson is a global healthcare company recognized for its contributions to Innovative Medicine and MedTech. Its safety operations support global drug development, ensuring that patient safety data is accurate, timely, and compliant with regulatory expectations. The Hyderabad site supports large-scale pharmacovigilance programs, technology upgrades, and capability transformation across global safety teams.
Job Role & Responsibilities
The Associate Pharmacovigilance, ICSR role supports capability development and continuous improvement across global safety operations. The work combines scientific knowledge, operational judgment, and system-focused execution.
Key Responsibilities
- Support development and enhancement of ICSR tools, including automation and AI-enabled systems
- Collaborate with global Case Management teams for capability rollout and operational readiness
- Drive governance support, training activities, and performance monitoring frameworks
- Apply pharmacovigilance knowledge to validate data accuracy and workflow alignment
- Identify process gaps, escalate issues, and support corrective action planning
- Support protocol-related and capability‑linked activities across case-management workflows
- Design and execute structured testing scenarios: create realistic ICSR cases, write test scripts, and validate functionality, data integrity, and end‑to‑end process alignment
Professional Expectations
- Ability to work independently across remote and cross-regional environments
- Strong problem‑solving mindset with structured escalation practices
- High level of professionalism, accountability, and process compliance
- Collaborative communication with cross-functional and multinational teams
Eligibility / Qualifications
Required Education
Accepted fields include:
B.Sc, M.Sc, B.Pharm, M.Pharm, Pharm.D, Nursing, MBBS, Biotechnology, Biochemistry, Biomedical Sciences, Life Sciences, Clinical Research.
Required Experience
- 2–5 years of pharmacovigilance or case‑management experience
- Knowledge of ICSR lifecycle steps: intake, processing, reporting
- Understanding of seriousness, causality, expectedness, MedDRA
- Experience with process improvement or automation initiatives in a regulated environment
- Hands-on experience writing or executing test scripts and case-testing scenarios
Preferred Qualifications
- Familiarity with Argus, ArisGlobal LifeSphere, or other safety databases
- Exposure to automation, GenAI, or workflow optimization
- Understanding of metrics, RCA, QMS, and compliance frameworks
Behavioral Competencies
Candidates should demonstrate:
- Independent decision-making
- Critical thinking and analytical ability
- Strong documentation skills
- Collaborative, respectful communication
- Adaptability and a positive, solution-oriented mindset
Location & Salary
- Location: Hyderabad, Andhra Pradesh, India
- Work Pattern: Hybrid
- Salary: Competitive, based on experience, technical skills, and safety-system exposure
Application Process
Applications must be submitted online through the Johnson & Johnson official career portal.
Apply here: https://www.careers.jnj.com/en/jobs/r-045362/associate-pharmacovigilance-icsr-hyderabad/?source=LinkedIn
Include a detailed resume highlighting ICSR experience, case-management exposure, and system-testing projects.
FAQs
Who is eligible for this role?
Professionals with 2–5 years of pharmacovigilance or ICSR experience.
Is this a case-processing role?
It supports ICSR capability development and testing but requires strong knowledge of ICSR processing steps.
Does the job involve global collaboration?
Yes. The role supports teams across multiple regions.
Which systems are preferred?
Argus, ArisGlobal LifeSphere, or similar global safety databases.
What education background is required?
Life Sciences, Pharmacy, Nursing, Medicine, or related disciplines.
Summary Table
| Category | Details |
|---|---|
| Company | Johnson & Johnson, Hyderabad |
| Vacancies | Associate Pharmacovigilance, ICSR |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Pharm.D, Nursing, MBBS, Biotechnology, Biochemistry, Biomedical Sciences, Life Sciences, Clinical Research |
| Experience | 2–5 years in pharmacovigilance or ICSR operations |
To apply for this job please visit www.careers.jnj.com.
