Drug Safety Associate Jobs at Vizen Life Sciences Hyderabad for B.Pharm, M.Pharm, PharmD with 1–5 years experience.
Location: Hyderabad, India
Job Type: Full-Time
Industry: Pharmacovigilance / Drug Safety
Experience: 1–5 Years
Education: B.Pharm / M.Pharm / PharmD
Job Status: Verified Job
Application Mode: Online Application
Vizen Life Sciences Pvt Ltd is hiring a Drug Safety Associate (ICSR) to strengthen its pharmacovigilance and clinical safety operations. This role is ideal for professionals with hands-on experience in Individual Case Safety Report (ICSR) processing, case triage, medical coding, and safety database management.
This opportunity offers exposure to global safety processes, regulatory audits, and client interactions, making it a strong career move for candidates seeking long-term growth in drug safety. Drug Safety Associate Jobs at Vizen Life Sciences
About the Company
Vizen Life Sciences Pvt Ltd is a growing pharmaceutical and life sciences organization providing high-quality pharmacovigilance, regulatory, and clinical safety services. The company is known for its compliance-driven approach, strong quality systems, and focus on developing skilled professionals in drug safety and regulatory operations.
Job Details
- Job Title: Drug Safety Associate (ICSR)
- Company: Vizen Life Sciences Pvt Ltd
- Employment Type: Full-Time
- Work Location: Hyderabad, India
- Experience Required: 1–5 Years
- Functional Area: Pharmacovigilance / Drug Safety
- Education Qualification: B.Pharm / M.Pharm / PharmD
Job Description
The Drug Safety Associate (ICSR) will be responsible for end-to-end processing of adverse event reports in compliance with global pharmacovigilance regulations. The role involves case intake, triage, data entry, medical coding, narrative writing, and follow-up management while ensuring quality, accuracy, and regulatory timelines. Drug Safety Associate Jobs at Vizen Life Sciences
This position requires strong knowledge of ICSR workflows, safety databases, MedDRA and WHO-DD coding, and regulatory requirements across different regions. Drug Safety Associate Jobs at Vizen Life Sciences
Key Responsibilities
- Triage incoming adverse event reports for validity, completeness, and legibility
- Perform accurate ICSR booking and data entry in the safety database
- Manage follow-up requests and resolve case-level queries
- Perform medical coding using MedDRA and WHO-DD dictionaries
- Prepare clear, concise, and compliant case narratives
- Conduct literature searches to identify reportable adverse events
- Participate in client communications and meetings as required
- Support regulatory audits and inspections, including preparation and follow-up activities
- Ensure compliance with global pharmacovigilance regulations and internal SOPs
Drug Safety Associate Jobs at Vizen Life Sciences
Skills / Qualifications
- B.Pharm, M.Pharm, or PharmD qualification
- 1–5 years of experience in pharmacovigilance or drug safety (ICSR processing)
- Hands-on experience with safety databases and literature surveillance
- Strong understanding of global PV regulations and guidelines
- Excellent written and verbal communication skills
- Strong analytical, organizational, and problem-solving abilities
- Ability to work independently and collaborate with cross-functional teams
- High attention to detail and quality standards
Drug Safety Associate Jobs at Vizen Life Sciences
Benefits / Perks
- Exposure to complete ICSR lifecycle management
- Opportunity to work on regulatory audits and inspections
- Professional and collaborative pharmacovigilance environment
- Skill enhancement in global drug safety operations
- Long-term career growth in clinical safety and pharmacovigilance
Drug Safety Associate Jobs at Vizen Life Sciences
Why You Should Join
Joining Vizen Life Sciences means working in a quality-driven pharmacovigilance setup where your expertise directly contributes to patient safety and regulatory compliance. The organization offers structured learning, hands-on exposure to global safety processes, and opportunities to grow within the drug safety domain. Drug Safety Associate Jobs at Vizen Life Sciences
How to Apply
Interested candidates can apply through the official advertisement application link provided by Vizen Life Sciences. Ensure your updated resume highlights relevant pharmacovigilance and ICSR experience before applying.
FAQs
Who can apply for the Drug Safety Associate (ICSR) role?
Candidates with B.Pharm, M.Pharm, or PharmD qualifications and 1–5 years of drug safety experience can apply.
Is this role suitable for freshers?
No, this position requires prior experience in ICSR processing or pharmacovigilance.
What tools and systems will I work on?
You will work with safety databases, MedDRA, WHO-DD coding systems, and literature surveillance tools.
Is this a full-time role?
Yes, this is a full-time, on-site position based in Hyderabad.
Does this role involve regulatory audits?
Yes, the role includes supporting regulatory audits and inspections as part of the pharmacovigilance function.
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