If you are a recent M.Pharm, Pharm D, or BDS graduate (2024–2026 pass-out) looking to start your career in pharmacovigilance and drug safety, this opportunity could be your ideal entry point into the clinical research industry. 🌍💊
A leading global Clinical Research Organization (CRO), Parexel, is hiring for the role of Patient Safety Associate I at its Hyderabad and Mohali offices (office-based role) on a 1-year contract basis.
This position is specially designed for freshers who want to build a strong foundation in ICSR processing, regulatory reporting, and global drug safety operations.
🌟 About the Company
Parexel is a globally recognized CRO supporting pharmaceutical, biotechnology, and medical device companies in developing life-changing therapies.
From clinical trials to regulatory consulting and safety monitoring, the organization plays a crucial role in improving global healthcare outcomes. 🌎✨
Working here means contributing directly to patient safety and global therapy development.
🧾 Job Overview
- Position: Patient Safety Associate I
- Location: Hyderabad / Mohali (Office-Based)
- Experience: Fresher
- Contract: 1 Year
This role focuses on pharmacovigilance operations including:
- Individual Case Safety Report (ICSR) processing
- Safety submissions
- Literature review
- Regulatory support
🔬 Key Responsibilities
1️⃣ ICSR Processing
This is the core of pharmacovigilance.
- Monitoring incoming adverse event reports 📩
- Performing literature searches and identifying valid cases
- Data entry into safety databases
- Ensuring correct MedDRA coding
- Preparing medically accurate case narratives
- Conducting quality checks
- Managing follow-ups and queries
- Supporting compliance with global reporting timelines
You’ll learn how to ensure adverse drug reactions (ADRs) are properly documented and reported to regulatory authorities worldwide.
2️⃣ Safety Submissions
- Submitting ICSRs and periodic safety reports
- Tracking regulatory reporting timelines
- Maintaining compliance metrics
- Supporting audits and inspections
This provides exposure to global drug safety regulations and ICH guidelines.
3️⃣ Literature Search & Review 📚
- Screening scientific journals for safety signals
- Identifying adverse reactions in published literature
- Maintaining search strategies
- Supporting signal detection activities
This builds your analytical and medical evaluation skills.
4️⃣ Affiliate & Regulatory Support 🌐
- Assisting communication with global affiliates
- Supporting product registration activities
- Managing regulatory intelligence updates
- Updating regulatory databases
You’ll gain exposure to international pharmacovigilance requirements.
🎓 Eligibility Criteria
Open to:
- M.Pharm
- Pharm D
- BDS
- Graduates from 2024, 2025, or 2026
✔️ Required Skills
- Basic knowledge of pharmacovigilance
- Strong communication skills
- Understanding of healthcare terminology
- MS Office proficiency
- Willingness to learn global safety regulations
Freshers with internships in PV, clinical research, or hospitals will have an added advantage.
💡 Why This Role is Perfect for Freshers
Starting in pharmacovigilance without experience can be challenging. This role is structured to:
✅ Provide hands-on ICSR training
✅ Teach global safety regulations
✅ Offer exposure to audits & compliance
✅ Develop regulatory intelligence skills
✅ Build a strong drug safety foundation
📈 Career Growth After 1–2 Years
You can transition into roles like:
- Drug Safety Associate
- Senior PV Executive
- Safety Reporting Specialist
- Regulatory Affairs Associate
- Signal Detection Analyst
Pharmacovigilance offers stable, global, and recession-resistant career growth. 🌎📊
🏢 Work Location Advantage
Both Hyderabad and Mohali are fast-growing hubs for clinical research and pharmacovigilance jobs in India.
Working in these cities gives exposure to:
- Multinational CRO environments
- Global regulatory systems
- Strong professional networking
📈 Career Scope in Pharmacovigilance
With increasing regulatory focus on patient safety worldwide, professionals skilled in:
- ICSR processing
- MedDRA coding
- Regulatory submissions
- Safety database management
- Literature screening
are in high demand across pharmaceutical and CRO companies.
This role can be your entry ticket into the global clinical research industry. 🎟️✨
📝 Final Thoughts
If you’re passionate about drug safety, regulatory compliance, and improving patient well-being, this Patient Safety Associate I role at Parexel is a strong starting point.
For fresh graduates, entering a reputed CRO like Parexel can significantly enhance your credibility and long-term career prospects in pharmacovigilance.
