Vizen Life Sciences hiring Drug Safety Associate (ICSR)
- Company Overview
- Job Role & Responsibilities
- ICSR Processing and Case Management
- Literature and Safety Surveillance
- Client Interaction and Compliance
- Skills and Competencies
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirements
- Location & Salary
- Application Process
- FAQs – Drug Safety Associate (ICSR)
- Who can apply for this Drug Safety Associate role?
- Is this role suitable for freshers?
- What type of work does ICSR involve?
- Does the role involve audits and inspections?
- What are the growth opportunities?
- Summary Table
Drug Safety Associate Vacancy Pune | BPharm MPharm
Vizen Life Sciences hiring Drug Safety Associate ICSR. BPharm/MPharm/PharmD with 1–3 years experience.
Vizen Life Sciences Pvt Ltd is hiring a Drug Safety Associate (ICSR) for professionals looking to strengthen their career in pharmacovigilance and clinical safety operations. This full-time role is suitable for candidates with hands-on experience in individual case safety report processing, safety database activities, and regulatory-compliant drug safety workflows. The position offers exposure to global pharmacovigilance practices, client interactions, audits, and inspections, making it a strong opportunity for early- to mid-level drug safety professionals.
Company Overview
Vizen Life Sciences Pvt Ltd is a growing life sciences and pharmacovigilance services organization supporting pharmaceutical, biotechnology, and healthcare companies. The company focuses on delivering high-quality drug safety, regulatory compliance, and clinical support services aligned with global regulatory expectations.
With a strong emphasis on quality, compliance, and client satisfaction, Vizen Life Sciences works closely with sponsors and CRO partners to ensure patient safety and data integrity across clinical and post-marketing activities. The organization provides structured learning, hands-on exposure, and long-term growth opportunities for professionals in pharmacovigilance and drug safety.
Job Role & Responsibilities
The Drug Safety Associate (ICSR) will be responsible for end-to-end processing of individual case safety reports and supporting pharmacovigilance activities in compliance with global regulatory standards. The role requires accuracy, attention to detail, and strong communication skills.
ICSR Processing and Case Management
- Triage incoming safety reports for completeness, validity, and legibility
- Perform case booking and data entry of safety reports into the pharmacovigilance database
- Code adverse events, medical history, and medications using standard dictionaries
- Write clear, accurate, and compliant case narratives
- Request and manage follow-ups to obtain missing or additional safety information
Literature and Safety Surveillance
- Perform literature searches to identify potential adverse event reports
- Review and document literature findings in line with pharmacovigilance requirements
- Support routine safety surveillance activities as assigned
Client Interaction and Compliance
- Participate in client meetings and discussions related to drug safety activities
- Support preparation for audits and regulatory inspections
- Assist in follow-up activities after audits or inspections
- Ensure adherence to internal SOPs and global pharmacovigilance guidelines
Skills and Competencies
- Strong analytical and problem-solving skills
- Ability to perform safety database searches and scientific literature reviews
- Excellent written and verbal communication skills
- Client-focused approach with attention to quality and timelines
- Ability to work in a regulated, process-driven environment
Eligibility / Qualifications
Educational Qualification
Candidates must hold one of the following qualifications:
- BPharm, MPharm, or PharmD
Relevant courses include: BPharm, MPharm (Pharmacology, Pharmaceutics), PharmD, MSc Pharmacology, MSc Clinical Research
Experience Requirements
- 1 to 3 years of experience in Drug Safety or Pharmacovigilance
- Hands-on experience in ICSR processing and safety database activities
- Exposure to audits, inspections, or client interactions is an advantage
Location & Salary
- Job Location: Not specified by employer
- Employment Type: Full-time
- Salary: As per industry standards and experience
This role offers stable career growth in pharmacovigilance with exposure to global safety operations.
Application Process
Interested and eligible candidates can apply directly through the official company portal using the link below:
Apply here: https://vizenlifesciences.keka.com/careers/jobdetails/43047?source=linkedin
Early applications are encouraged as shortlisting may begin immediately.
FAQs – Drug Safety Associate (ICSR)
Who can apply for this Drug Safety Associate role?
Candidates with BPharm, MPharm, or PharmD qualifications and 1–3 years of drug safety experience can apply.
Is this role suitable for freshers?
No. Prior experience in pharmacovigilance or ICSR processing is required.
What type of work does ICSR involve?
ICSR work includes case intake, data entry, coding, narrative writing, follow-ups, and literature review.
Does the role involve audits and inspections?
Yes. The role supports preparation for and participation in audits and regulatory inspections.
What are the growth opportunities?
This role provides a strong foundation for senior drug safety, signal management, and pharmacovigilance specialist positions.
Summary Table
| Company | Vizen Life Sciences Pvt Ltd |
|---|---|
| Vacancies | Drug Safety Associate (ICSR) |
| Required Education | BPharm, MPharm, PharmD |
| Experience | 1–3 years in Drug Safety / Pharmacovigilance |
To apply for this job please visit vizenlifesciences.keka.com.
