Parexel Fresher Pharmacovigilance Hiring | Patient Safety Associate
- Parexel Hiring Patient Safety Associate Freshers | Pharmacovigilance Jobs in Mohali
- Company Overview
- Job Role & Responsibilities
- ICSR Processing & Drug Safety
- Safety Reporting & Compliance
- Literature Review & Signal Detection
- Regulatory & Operational Support
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is ICSR processing?
- 3. What career growth can I expect?
- 4. What skills are important?
- Summary
Parexel Hiring Patient Safety Associate Freshers | Pharmacovigilance Jobs in Mohali
A high-impact opportunity is now open for candidates aiming to build a career in pharmacovigilance and drug safety. Parexel is hiring Patient Safety Associate I for its Mohali location, offering a strong entry point into global clinical research and safety reporting operations.
This role is ideal for freshers and early-career professionals from life sciences backgrounds who want hands-on experience in ICSR processing, safety data management, regulatory submissions, and global pharmacovigilance systems.
With exposure to international regulatory guidelines and real-world clinical safety data, this position provides a solid foundation for long-term growth in clinical research, drug safety, and regulatory affairs.
Company Overview
Parexel is a globally recognized clinical research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in developing and delivering life-changing therapies. With deep expertise across clinical trials, regulatory consulting, pharmacovigilance, and market access, Parexel plays a key role in advancing global healthcare innovation.
The company is known for its patient-focused approach, strong compliance culture, and commitment to high-quality clinical research and safety standards. Working at Parexel offers exposure to global clinical development projects and regulatory environments.
Job Role & Responsibilities
As a Patient Safety Associate, you will be responsible for supporting pharmacovigilance activities, including case processing, safety reporting, and compliance with global regulatory requirements.
ICSR Processing & Drug Safety
- Monitor and triage adverse event reports from multiple sources
- Perform data entry and case processing in safety databases
- Ensure accurate MedDRA coding and case documentation
- Prepare and review adverse event narratives
- Conduct follow-ups and query management for incomplete cases
Safety Reporting & Compliance
- Support submission of Individual Case Safety Reports (ICSRs) to regulatory authorities
- Maintain compliance with global pharmacovigilance guidelines (ICH, GCP)
- Assist in preparation of periodic safety reports and regulatory documentation
- Support audit and inspection readiness activities
Literature Review & Signal Detection
- Conduct scientific literature searches for safety signals
- Screen and evaluate articles for adverse drug reactions
- Support signal detection and risk assessment activities
Regulatory & Operational Support
- Maintain regulatory databases and safety documentation
- Assist in global regulatory submissions and compliance tracking
- Coordinate with cross-functional teams for safety data management
Eligibility / Qualifications
Educational Qualification:
M.Pharmacy, B.Pharmacy, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry
Relevant Courses:
Pharmacovigilance, Clinical Research, Drug Safety, Regulatory Affairs, Pharmaceutical Sciences
Experience Required:
- Freshers and candidates with basic pharmacovigilance knowledge can apply
Skills Required:
- Basic understanding of pharmacovigilance and drug safety processes
- Knowledge of medical terminology and clinical data
- Strong analytical and problem-solving skills
- Attention to detail and documentation accuracy
- Good communication and teamwork abilities
Location & Salary
- Location: Mohali, India
- Job Type: Full-time
- Salary: As per industry standards
This role provides strong exposure to global pharmacovigilance operations, making it a valuable opportunity for candidates targeting careers in drug safety, clinical data management, and regulatory compliance.
Application Process
Interested candidates can apply through the official Parexel careers portal:
Early application is recommended due to high demand for pharmacovigilance roles.
Why This Role Matters in Healthcare
Patient Safety Associates play a critical role in monitoring drug safety and ensuring that adverse events are properly documented and reported. Their work directly contributes to patient safety, regulatory compliance, and the development of safer medicines worldwide.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
Yes, freshers with life science backgrounds can apply.
2. What is ICSR processing?
It involves handling adverse event reports and ensuring accurate safety data reporting.
3. What career growth can I expect?
You can grow into roles like Drug Safety Associate, PV Specialist, or Safety Scientist.
4. What skills are important?
Attention to detail, regulatory knowledge, and data handling skills.
Summary
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Patient Safety Associate |
| Required Education | M.Pharm, B.Pharm, MSc |
| Experience | Freshers / Entry-level |
To apply for this job please visit wd1.myworkdaysite.com.
