Drug Safety Associate Jobs at Vizen Life Sciences Pharmacovigilance Hiring for B.Pharm M.Pharm PharmD candidates with pharmacovigilance experience. Apply now.
Introduction
Vizen Life Sciences Pvt Ltd is currently hiring for the position of Drug Safety Associate (ICSR), offering an excellent opportunity for candidates interested in pharmacovigilance and drug safety operations. This role is suitable for professionals who have experience in case processing and safety data management.
Candidates with a background in pharmacy and a keen interest in adverse event reporting and regulatory compliance can leverage this opportunity to grow in the drug safety domain.
Company Overview
Vizen Life Sciences Pvt Ltd is a growing organization specializing in pharmacovigilance, regulatory support, and clinical research services. The company focuses on delivering high-quality safety and compliance solutions to pharmaceutical clients.
With a commitment to accuracy, regulatory standards, and client satisfaction, Vizen Life Sciences provides a professional environment for individuals to build expertise in drug safety and global pharmacovigilance practices.
Job Overview
| Job Title | Drug Safety Associate (ICSR) |
|---|---|
| Company Name | Vizen Life Sciences Pvt Ltd |
| Location | Not Specified |
| Employment Type | Full-Time |
| Qualification | B.Pharm / M.Pharm / Pharm.D |
| Experience | 1–3 Years |
| Salary | As per company norms |
| Application Mode | Not Specified |
Job Location & Employment Type
This is a full-time role in the pharmacovigilance domain. The exact job location has not been specified, and candidates may need to confirm this during the application process.
Open Positions / Department Details
- Department: Pharmacovigilance / Drug Safety
- Role: Drug Safety Associate (ICSR Processing)
This role focuses on Individual Case Safety Report (ICSR) handling and safety database management.
Key Roles & Responsibilities
- Review incoming safety reports for completeness, accuracy, and validity
- Perform case booking and data entry into safety databases
- Manage follow-up queries and ensure proper case documentation
- Code adverse event data using standard medical dictionaries
- Prepare detailed and accurate case narratives
- Conduct literature searches for safety-related information
- Participate in client meetings when required
- Support audit and inspection activities including preparation and follow-up
- Maintain compliance with pharmacovigilance guidelines and timelines
Eligibility Criteria
Education:
- B.Pharm, M.Pharm, or Pharm.D
Experience:
- 1 to 3 years of experience in pharmacovigilance or drug safety operations
- Experience in ICSR processing is preferred
Skills Required:
Technical Skills:
- Knowledge of pharmacovigilance processes and ICSR workflows
- Experience with safety databases and coding systems
- Ability to perform literature and database searches
- Understanding of regulatory requirements and reporting standards
Soft Skills:
- Strong analytical and problem-solving abilities
- Excellent written and verbal communication skills
- Attention to detail and accuracy
- Client-focused approach and teamwork skills
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in pharmacovigilance and drug safety domain
- Exposure to global safety reporting standards
- Career growth in clinical research and regulatory fields
- Learning opportunities in audits, inspections, and compliance
Selection Process
The hiring process may include:
- Resume screening
- Technical interview focusing on pharmacovigilance knowledge
- Assessment of ICSR handling experience
- HR discussion for final selection
Shortlisted candidates will be contacted for further rounds.
How to Apply
The application mode is not specified. Candidates are advised to check the official company website or job portal where the job was listed for application details.
Why Apply for This Pharma Job?
This role is ideal for candidates aiming to build or advance their career in pharmacovigilance. Working as a Drug Safety Associate provides exposure to real-world safety case processing, regulatory compliance, and global reporting systems.
Candidates will gain hands-on experience in ICSR management, narrative writing, and safety database handling, which are critical skills in the pharmaceutical and clinical research industries.
For professionals looking to establish themselves in drug safety and regulatory domains, this opportunity offers a strong foundation and long-term career potential.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
Eligible candidates with relevant pharmacovigilance experience are encouraged to apply at the earliest once the application details are confirmed. Early action can improve your chances of securing this role.
