Apply for Patient Safety Associate I at Parexel 2026. Check eligibility, salary, job role details, and application process today online.
Introduction
If you are looking to build a career in pharmacovigilance and drug safety, the Patient Safety Associate I at Parexel role offers an excellent opportunity for freshers and early professionals. This position provides hands-on exposure to global safety reporting, regulatory compliance, and clinical safety operations. Candidates from life sciences backgrounds can gain valuable industry experience while working with an internationally recognized CRO.
Job Overview
| Details | Information |
|---|---|
| Job Title | Patient Safety Associate I |
| Company Name | Parexel |
| Location | Hyderabad, Mohali (India) |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Drug Safety |
| Experience Required | Freshers / Entry-Level |
| Education | Life Sciences / Pharmacy / Biomedical Sciences |
| Salary | As per company norms |
Company Overview
Parexel is a globally established clinical research organization (CRO) that specializes in clinical trials, regulatory consulting, and drug development solutions. The company is known for supporting pharmaceutical and biotechnology organizations in bringing new therapies to market efficiently. With a strong emphasis on patient safety and innovation, Parexel offers a collaborative environment for professionals looking to grow in clinical research and pharmacovigilance.
Job Location & Employment Type
This role is available in multiple Indian locations, including Hyderabad and Mohali. It is a full-time opportunity, ideal for candidates seeking long-term careers in pharmacovigilance and clinical safety.
Open Positions / Department Details
The position falls under the Pharmacovigilance (PV) or Drug Safety department, focusing on:
- Individual Case Safety Report (ICSR) processing
- Safety submissions and compliance
- Literature review and signal detection
- Regulatory support and reporting
Key Roles & Responsibilities
General Responsibilities
- Gain knowledge of drug safety profiles, labeling, and global regulations
- Follow company procedures and workflows for safety reporting
- Assist in audit preparation and compliance tracking
- Maintain accurate documentation and records
ICSR Processing
- Monitor incoming safety reports from multiple sources
- Perform data entry and case processing in safety databases
- Validate case information for accuracy and completeness
- Conduct MedDRA coding and ensure regulatory compliance
- Prepare case narratives and follow-up queries
Safety Submissions
- Submit safety reports to regulatory authorities and stakeholders
- Manage reporting timelines and ensure compliance
- Support global safety reporting procedures
- Track submission metrics and compliance data
Literature Review
- Conduct literature searches for adverse drug reactions
- Review scientific articles for safety signals
- Maintain search strategies and databases
- Identify potential risks and escalate findings
Affiliate & Regulatory Support
- Assist in communication with global and local teams
- Support regulatory submissions and product registrations
- Maintain safety databases and reporting systems
- Monitor country-specific regulatory requirements
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Pharmacy
- Biotechnology
- Microbiology
- Biochemistry
- Life Sciences or related fields
Experience
- Freshers can apply
- Prior exposure to pharmacovigilance or healthcare is an advantage
Skills Required
- Basic understanding of drug safety and pharmacovigilance
- Strong analytical and problem-solving skills
- Good communication and teamwork abilities
- Familiarity with MS Office and basic computer skills
- Willingness to learn regulatory guidelines (ICH, global standards)
Salary & Benefits
- Salary: As per company norms
- Additional Benefits:
- Professional training and development
- Exposure to global clinical projects
- Career growth in pharmacovigilance
- Work in an international CRO environment
Selection Process
The selection process typically includes:
- Online application submission
- Resume screening
- HR interview
- Technical/functional interview
- Final selection
How to Apply
Candidates need to apply through the official online application portal of Parexel. Ensure that your resume is updated with relevant educational and skill details before applying.
Important Dates
- Application Start Date: Already Open
- Last Date to Apply: Not specified (Apply as early as possible)
Why Apply for This Job?
The Patient Safety Associate I at Parexel role is ideal for candidates aiming to enter the pharmacovigilance field. It offers:
- Entry into the global clinical research industry
- Hands-on experience in drug safety and regulatory reporting
- Opportunity to work with international clients
- Structured training and career advancement pathways
- Exposure to real-world clinical data and safety systems
This role can serve as a strong foundation for future growth in clinical research, regulatory affairs, or advanced pharmacovigilance positions.
FAQs
1. Who can apply for Patient Safety Associate I at Parexel?
Candidates with degrees in pharmacy, life sciences, or biomedical sciences can apply. Freshers are eligible.
2. Is prior experience required for this role?
No, this is an entry-level position. However, basic knowledge of pharmacovigilance is beneficial.
3. What is the salary for this position?
Salary is offered as per company norms and may vary based on qualifications and skills.
4. What skills are important for this job?
Analytical thinking, communication skills, basic drug safety knowledge, and attention to detail are important.
5. How can I apply for this job?
You can apply online through the official Parexel careers page.
Conclusion
The Patient Safety Associate I at Parexel 2026 opportunity is a great starting point for candidates interested in pharmacovigilance and clinical safety. With structured training, global exposure, and strong career growth prospects, this role can help you build a successful career in the pharmaceutical industry. Interested candidates should apply as soon as possible to secure their chance.
Disclaimer
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