Looking for pharma jobs, pharmacovigilance jobs, QA jobs, QC jobs, production jobs, or pharmaceutical careers in India? Parexel is hiring Patient Safety Associate I professionals for its Mohali and Hyderabad locations. Eligible 2025 and 2026 graduates can apply for this exciting opportunity in global drug safety and pharmacovigilance.
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About the Company
Parexel is a globally recognized clinical research organization (CRO) dedicated to improving patient health through innovative clinical development solutions.
The company supports pharmaceutical, biotechnology, and medical device organizations across the entire product lifecycle, from clinical trials to regulatory consulting and market access services.
With a strong commitment to regulatory compliance, scientific excellence, and patient safety, Parexel has built a reputation as one of the world’s leading healthcare and life sciences organizations.
Its global presence, cutting-edge technologies, and collaborative work culture make it an ideal workplace for professionals seeking long-term growth in the pharmaceutical and clinical research industries.
Job Details
- Company Name: Parexel
- Position: Patient Safety Associate I
- Experience: Freshers and entry-level candidates; internships preferred
- Qualification: Master’s Degree in Life Sciences, Pharmacy, or related field, PharmD, BDS
- Eligible Batch: 2025 and 2026 Graduates
- Location: Mohali, India; Hyderabad, India
- Work Type: On-site
Job Description
Parexel is expanding its pharmacovigilance and drug safety operations team and is seeking highly motivated professionals to support global patient safety activities.
This role offers an excellent opportunity to work in clinical research, safety reporting, regulatory compliance, and pharmacovigilance operations.
Patient Safety Associate I
- Department: Pharmacovigilance / Drug Safety
- Market: Global Clinical Research
- Role: Patient Safety Associate I
- Experience: Entry-level; internship experience preferred
- Education/Qualification: Master’s Degree in Life Sciences, Pharmacy, PharmD, BDS, or related field
Skills/Qualifications
- Basic knowledge of pharmacovigilance principles
- Understanding of ICH guidelines
- Knowledge of global safety reporting requirements
- Familiarity with MedDRA coding
- Strong analytical and problem-solving skills
- Excellent attention to detail
- Effective communication abilities
- Good organizational and time-management skills
- Proficiency in Microsoft Office applications
- Familiarity with safety databases is advantageous
- Ability to manage multiple deadlines
- Strong teamwork and collaboration skills
Key Responsibilities
- Process Individual Case Safety Reports (ICSRs)
- Perform safety data entry and coding
- Write and review case narratives
- Conduct quality checks on safety reports
- Review scientific literature for safety signals
- Support regulatory safety submissions
- Track compliance and reporting timelines
- Assist with signal detection activities
- Maintain safety documentation accuracy
- Coordinate follow-up and query management
- Support aggregate safety reports
- Monitor regulatory reporting updates
- Participate in audits and inspections
- Collaborate with internal stakeholders
- Support client communication activities
Benefits/Perks
- Opportunity to work with a global CRO
- Exposure to international pharmacovigilance projects
- Structured learning and development programs
- Strong career growth opportunities
- Collaborative and inclusive work environment
- Competitive compensation package
- Industry-leading training and mentorship
- Experience with global regulatory standards
- Professional development opportunities
- Long-term career stability in healthcare research
How to Apply
Interested candidates can apply directly through the official Parexel Careers Portal before the application deadline.
Career Page: https://jobs.parexel.com
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Parexel career page.
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For additional pharmaceutical career opportunities, candidates can also explore opportunities through Pharma Recruiter at https://pharmarecruiter.in
Apply now and start your career journey with one of the world’s leading clinical research organizations in pharmacovigilance and patient safety.
Why You Should Join
Parexel offers a unique opportunity to contribute to global healthcare advancements while building a rewarding career in pharmacovigilance. Employees benefit from a culture of innovation, regulatory excellence, and continuous learning.
FAQs
Who is eligible to apply for the Patient Safety Associate I role?
Candidates with a Master’s Degree in Life Sciences, Pharmacy, PharmD, BDS, or related fields who graduated in 2025 or 2026 are eligible.
Is prior pharmacovigilance experience required?
No. Fresh graduates can apply. However, internships or exposure to pharmacovigilance, clinical research, or healthcare environments are preferred.
Is there a walk-in interview for this position?
No walk-in interview details have been announced. Applications must be submitted through the official Parexel Careers Portal.
What career growth opportunities are available?
Employees can advance into pharmacovigilance, drug safety, regulatory affairs, clinical research, quality assurance, and leadership roles through structured development programs.
