AlphaCure Life Sciences. The company is currently recruiting experienced candidates for Drug Safety Associate roles specializing in Medical Literature Monitoring and Periodic Adverse Drug Experience Reports (PADER).
This is an excellent opportunity for B.Pharm, M.Pharm, and Pharm.D graduates with 3–5 years of relevant pharmacovigilance experience to work in a professional, growth-oriented environment and contribute to global drug safety operations.
Job Overview
| Particulars | Details |
|---|---|
| Company Name | AlphaCure Life Sciences |
| Job Role | Drug Safety Associate |
| Specialization | Medical Literature Monitoring, PADER |
| Location | Kondapur |
| Experience | 3–5 Years |
| Qualification | B.Pharm / M.Pharm / Pharm.D |
| Work Mode | Work From Office |
| Shift Timing | 2:00 PM – 11:00 PM |
| Salary | Best in Industry |
| Application Mode |
About AlphaCure Life Sciences
AlphaCure Life Sciences is a growing healthcare and pharmacovigilance-focused organization providing regulatory, drug safety, and medical information services to pharmaceutical and biotechnology companies. The company offers professionals opportunities to work on global pharmacovigilance projects while developing expertise in drug safety reporting and compliance.
Key Responsibilities
Drug Safety Associate – Medical Literature Monitoring
- Conduct systematic literature searches and monitoring activities.
- Review scientific publications for adverse event information.
- Identify, assess, and document safety-related information.
- Ensure compliance with global pharmacovigilance regulations.
- Maintain accurate documentation and reporting timelines.
Drug Safety Associate – PADER
- Prepare and review Periodic Adverse Drug Experience Reports (PADER).
- Analyze safety data and adverse event trends.
- Collaborate with cross-functional pharmacovigilance teams.
- Ensure timely submission of regulatory safety reports.
- Support signal detection and benefit-risk assessment activities.
Required Qualifications
Candidates applying for these pharmacovigilance jobs in Hyderabad should possess:
- B.Pharm, M.Pharm, or Pharm.D qualification.
- 3–5 years of relevant pharmacovigilance experience.
- Strong understanding of drug safety regulations and reporting requirements.
- Experience in Medical Literature Monitoring or PADER preparation.
- Excellent analytical and communication skills.
- Ability to work in a fast-paced regulatory environment.
Preferred Skills
- Pharmacovigilance case processing knowledge.
- Regulatory compliance expertise.
- Literature review and medical writing capabilities.
- Safety database experience.
- Attention to detail and quality-focused approach.
Benefits
- Competitive salary package based on current CTC.
- Opportunity to work on global pharmacovigilance projects.
- Professional growth and career advancement.
- Exposure to experienced drug safety professionals.
- Dynamic and collaborative workplace environment.
Why This Opportunity Stands Out
The demand for experienced Drug Safety Associates continues to grow as pharmaceutical companies strengthen global pharmacovigilance systems. These Drug Safety Associate jobs in Hyderabad offer exposure to Medical Literature Monitoring and PADER activities, making them ideal for professionals looking to advance their careers in drug safety, pharmacovigilance, regulatory affairs, and medical writing.
How to Apply
Interested candidates meeting the eligibility criteria can send their updated CV to:
Email: hr@alphacurels.com
Job Location: Trendset Jayabheri Connect, Kondapur, Hyderabad, Telangana