SafeVig Solutions LLC, a leading life sciences and pharmacovigilance services company, is inviting applications for the position of Drug Safety Associate in Hyderabad, Telangana. This full-time onsite opportunity is ideal for pharmacy and life sciences professionals looking to build a career in pharmacovigilance, drug safety, medical review, case processing, and regulatory compliance.
With over 25 years of industry expertise, SafeVig Solutions delivers specialized pharmacovigilance, clinical operations, regulatory affairs, and medical affairs solutions to pharmaceutical and biotechnology companies worldwide. The company is recognized for its innovative safety platforms and patient-centric approach to global drug safety management.
Job Overview
| Details | Information |
|---|---|
| Position | Drug Safety Associate |
| Company | SafeVig Solutions LLC |
| Location | Hyderabad, Telangana, India |
| Job Type | Full-Time |
| Work Mode | On-site |
| Industry | Pharmacovigilance / Drug Safety |
| Qualification | Pharmacy or Related Life Sciences Degree |
| Experience | Freshers to Experienced Candidates |
| Department | Pharmacovigilance |
Key Responsibilities
As a Drug Safety Associate, selected candidates will be responsible for:
- Drafting and reviewing medical case narratives.
- Performing quality control checks on safety reports and pharmacovigilance data.
- Ensuring accuracy, consistency, and compliance of adverse event information.
- Supporting medical coding activities using standard dictionaries.
- Collaborating with regulatory affairs teams for safety submissions.
- Maintaining compliance with global pharmacovigilance regulations and safety standards.
- Assisting in case processing and safety data management activities.
- Supporting patient safety initiatives and risk management processes.
Required Qualifications
Candidates applying for the Drug Safety Associate role should possess:
- Bachelor’s or Master’s degree in Pharmacy, PharmD, Life Sciences, or a related discipline.
- Knowledge of pharmacovigilance principles and drug safety reporting.
- Experience in medical coding and case narrative writing is preferred.
- Strong quality control and documentation skills.
- Understanding of global regulatory affairs and safety guidelines.
- Excellent analytical, communication, and organizational skills.
- Ability to work effectively in a collaborative team environment.
Preferred Skills
- Pharmacovigilance case processing experience.
- Adverse event reporting knowledge.
- Medical review and safety database familiarity.
- Regulatory compliance understanding.
- Attention to detail and accuracy in safety documentation.
Why Join SafeVig Solutions?
SafeVig Solutions offers employees the opportunity to work with global pharmaceutical and biotechnology clients while contributing to patient safety initiatives worldwide.
Benefits
- Exposure to international pharmacovigilance projects.
- Career growth in drug safety and regulatory affairs.
- Learning opportunities with experienced industry professionals.
- Collaborative and innovation-driven work environment.
- Experience with advanced pharmacovigilance technologies and automation platforms.
About SafeVig Solutions LLC
SafeVig Solutions LLC is a trusted life sciences partner specializing in pharmacovigilance, clinical operations, regulatory affairs, medical affairs, and safety technology solutions. The company helps pharmaceutical and biotechnology organizations navigate complex global regulatory requirements while ensuring patient safety and operational excellence.
How to Apply
