Are you looking for Drug Safety Associate II jobs in Hyderabad? SafeVig Solutions Pvt. Ltd., a rapidly growing Contract Research Organization (CRO), is hiring experienced Pharmacovigilance professionals for the position of Drug Safety Associate II (DSA II). Candidates with 2–5 years of experience in ICSR case processing, MedDRA coding, narrative writing, and pharmacovigilance operations are encouraged to apply.
This is an excellent opportunity for professionals seeking Pharmacovigilance jobs in Hyderabad, exposure to global drug safety projects, and career growth within a quality-focused CRO environment.
Job Overview
| Details | Information |
|---|---|
| Position | Drug Safety Associate II (DSA II) |
| Company | SafeVig Solutions Pvt. Ltd. |
| Location | Hyderabad, Telangana |
| Employment Type | Full-Time |
| Experience Required | 2–5 Years |
| Industry | Pharmacovigilance / Drug Safety |
| Work Mode | Work from Office |
About SafeVig Solutions
SafeVig Solutions Pvt. Ltd. is a growing CRO specializing in Pharmacovigilance, Clinical Research, Regulatory Affairs, and Safety Technology services. The organization supports pharmaceutical and biotechnology companies through compliant, quality-driven, and efficient safety solutions.
Key Responsibilities
As a Drug Safety Associate II, you will:
- Perform end-to-end ICSR case processing activities.
- Conduct data entry and quality review of adverse event reports.
- Perform MedDRA coding and medical assessment.
- Write and review case narratives.
- Process spontaneous, literature, clinical trial, and solicited cases.
- Ensure compliance with SOPs, client requirements, and global regulatory guidelines.
- Support literature surveillance activities.
- Maintain productivity and quality metrics.
- Participate in audits, quality reviews, and CAPA activities.
- Contribute to process improvement initiatives and project deliverables.
Educational Qualifications
Candidates should possess any of the following qualifications:
- M.Pharm
- Pharm.D
- B.Pharm
- Life Sciences
- Nursing
- Biotechnology
- Other Healthcare or Related Scientific Disciplines
Experience Required
- 2–5 years of Pharmacovigilance experience.
- Strong hands-on experience in ICSR case processing.
- Experience working with safety databases is preferred.
Preferred Safety Databases
- Argus Safety
- ARISg
- Veeva Safety
- Other Pharmacovigilance Safety Platforms
Required Skills
Successful candidates should demonstrate expertise in:
- ICSR Processing
- MedDRA Coding
- Narrative Writing
- Pharmacovigilance Regulations
- Case Assessment
- Literature Surveillance
- Attention to Detail
- Time Management
- Communication Skills
- Team Collaboration
Why Join SafeVig Solutions?
SafeVig offers employees:
- Exposure to global Pharmacovigilance projects.
- Opportunities to work with leading pharmaceutical and biotechnology clients.
- Continuous learning and professional development.
- Career growth in a rapidly expanding CRO.
- Collaborative and quality-focused work culture.
- Hands-on experience with advanced drug safety technologies.
How to Apply
Interested candidates can send their updated resume to:
📧 support@safevigsolutions.com
Applicants are advised to mention “Application for Drug Safety Associate II – Hyderabad” in the email subject line for faster processing.