Apply for Case Specialist Pharmacovigilance job at PLG India. Check eligibility, experience, remote work details, and application process now.
Introduction
If you are a pharmacy professional looking to grow in pharmacovigilance and drug safety, this opportunity can be a strong career move. The Case Specialist Pharmacovigilance Job at PLG is designed for experienced professionals who can handle vigilance case processing and safety data evaluation. With remote work flexibility and exposure to global safety standards, this role offers excellent scope for career development in drug safety and vigilance operations.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Case Specialist – Pharmacovigilance |
| Company Name | PLG |
| Location | India (Remote work possible) |
| Employment Type | Permanent |
| Department | Safety and Vigilance |
| Experience Required | 4–5 Years |
| Education | B.Pharm / M.Pharm (Pharmacist) |
| Salary | As per company norms |
Company Overview
PLG is a rapidly expanding life sciences consulting organization offering services in regulatory affairs, pharmacovigilance, and quality compliance. The company collaborates with global pharmaceutical clients to ensure drug safety, regulatory adherence, and lifecycle management. With a focus on innovation and compliance, PLG provides professionals with opportunities to work on international safety projects and develop specialized expertise.
Job Location & Employment Type
- Location: India
- Work Mode: Remote / Work-from-home
- Employment Type: Permanent
This role is suitable for candidates seeking flexibility while working on global pharmacovigilance processes.
Open Positions / Department Details
- Department: Safety and Vigilance
- Role Focus:
- Pharmacovigilance case processing
- Medical evaluation and safety reporting
- Quality control of vigilance data
Key Roles & Responsibilities
As a Case Specialist in Pharmacovigilance, your responsibilities will include:
- Performing quality checks of vigilance cases to ensure accuracy and compliance
- Conducting medical evaluation of adverse event reports
- Entering and managing safety data in databases or client-specific systems
- Following up on cases via email or phone for additional information
- Performing pre-analysis of complex cases before data entry
- Coding adverse events using standard medical dictionaries
- Assessing causality between drug exposure and reported events
- Determining seriousness and expectedness of adverse events
- Identifying reporting requirements for individual case safety reports (ICSRs)
- Reviewing and validating documents prepared by team members
- Closing vigilance cases after completion of evaluation
- Supporting implementation of ICSR and MLM filters
- Analyzing inclusion/exclusion criteria for regulatory cases (EV/MHRA)
- Providing medical information support when required
- Handling incoming safety-related calls
- Reviewing medical inquiries and quality complaints for safety signals
- Acting as a key contact for assigned clients
- Preparing and maintaining quality and compliance documentation
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm)
- Must be a qualified pharmacist
Experience
- 4–5 years of experience in pharmacovigilance or similar safety roles
- Experience in case processing and medical evaluation
Skills Required
- Knowledge of global pharmacovigilance regulations
- Experience with safety databases and coding dictionaries
- Strong analytical and medical evaluation skills
- Familiarity with ICSR processing and reporting requirements
- Proficiency in Microsoft Office tools
- Ability to manage multiple tasks efficiently
- Strong attention to detail and process-oriented approach
- Excellent communication and teamwork skills
- Flexibility in handling dynamic work environments
Salary & Benefits
- Salary: As per company norms
- Work-from-home flexibility
- Exposure to global pharmacovigilance systems
- Opportunity to work on international safety cases
- Career growth in drug safety and vigilance
- Supportive and collaborative work environment
Selection Process
The selection process generally includes:
- Resume screening
- Technical interview (Pharmacovigilance & case processing)
- Final HR discussion
Candidates with strong experience in vigilance case handling will be preferred.
How to Apply
- Apply through the official job portal (no email or walk-in details provided)
Important Dates
- Not specified (Apply early to increase selection chances)
Why Apply for This Job?
The Case Specialist Pharmacovigilance Job at PLG is an excellent opportunity for pharmacy professionals to deepen their expertise in drug safety and vigilance systems. The role offers hands-on experience in medical evaluation, adverse event processing, and global compliance standards.
Additionally, the remote work option allows flexibility while working on international projects, making it an ideal position for professionals seeking both work-life balance and career advancement in pharmacovigilance.
FAQs
1. What is the main role of a Case Specialist in Pharmacovigilance?
The role involves processing and evaluating adverse event cases, ensuring regulatory compliance, and maintaining safety data accuracy.
2. Is this a remote job?
Yes, this position allows remote work within India.
3. What qualification is required for this role?
Candidates must have a degree in Pharmacy (B.Pharm or M.Pharm).
4. How much experience is needed?
A minimum of 4–5 years of pharmacovigilance experience is required.
5. What skills are important for this job?
Key skills include medical evaluation, data analysis, regulatory knowledge, and strong communication abilities.
Conclusion
The Case Specialist Pharmacovigilance Job at PLG offers a promising career path for experienced pharmacy professionals. With global exposure, flexible work options, and opportunities to work on critical safety processes, this role is ideal for those aiming to excel in pharmacovigilance. Interested candidates should apply at the earliest.
Disclaimer
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