Parexel Fresher Pharmacovigilance Hiring Patient Safety Associate I
- Parexel Hiring Patient Safety Associate I – Freshers Eligible | Multiple Vacancies in Hyderabad, Bengaluru & Mohali
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Regulatory & Compliance Activities
- Literature & Safety Monitoring
- Additional Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Skills Required
- Experience
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is prior experience required?
- 3. What is the career scope after this role?
- 4. What skills are important for selection?
- 5. Is this a good entry-level pharma job?
- Summary Table
Parexel Hiring Patient Safety Associate I – Freshers Eligible | Multiple Vacancies in Hyderabad, Bengaluru & Mohali
Parexel is hiring Patient Safety Associate I professionals across Medical Sciences for multiple vacancies in Hyderabad, Bengaluru, and Mohali. This is an excellent opportunity for freshers and candidates with basic pharmacovigilance knowledge looking to build a career in drug safety, clinical research, and regulatory affairs. If you are from Life Sciences, Pharmacy, Biotechnology, or related backgrounds, this role offers a strong entry point into high-growth healthcare and pharmaceutical careers.
Company Overview
Parexel is a globally recognized clinical research organization (CRO) known for delivering advanced clinical development and pharmacovigilance solutions to pharmaceutical, biotechnology, and medical device companies. With a strong global presence, Parexel plays a key role in accelerating drug development and ensuring patient safety through robust clinical research and regulatory compliance systems.
The company is widely trusted for its expertise in clinical trials, regulatory consulting, and drug safety services, making it a preferred employer for professionals aiming to grow in the healthcare and life sciences industry.
Job Role & Responsibilities
As a Patient Safety Associate I, you will be involved in pharmacovigilance operations, focusing on drug safety data processing, adverse event reporting, and regulatory compliance activities. This role directly contributes to patient safety and global healthcare standards.
Core Responsibilities
- Monitor and process Individual Case Safety Reports (ICSRs) from multiple sources such as literature, databases, and regulatory platforms
- Perform accurate data entry and case processing in safety databases following SOPs and global guidelines
- Conduct MedDRA coding and ensure correct classification of adverse events
- Review and validate safety data for completeness, accuracy, and medical consistency
- Prepare adverse drug reaction (ADR) reports and safety narratives
- Manage follow-ups and queries related to safety cases
Regulatory & Compliance Activities
- Support submission of safety reports to global regulatory authorities and ethics committees
- Assist in maintaining compliance with pharmacovigilance regulations and reporting timelines
- Participate in audits, inspections, and documentation processes
- Maintain accurate safety reporting metrics and compliance records
Literature & Safety Monitoring
- Conduct scientific literature searches to identify potential adverse drug reactions
- Screen and review medical publications for safety signals and emerging risks
- Support signal detection activities and safety evaluations
Additional Responsibilities
- Collaborate with global teams and local affiliates for safety data exchange
- Assist in regulatory submissions, product registrations, and lifecycle management
- Support database updates, safety reporting systems, and documentation
- Participate in training programs and continuous learning modules
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in Life Sciences or related disciplines.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Nursing, or equivalent
Skills Required
- Basic understanding of pharmacovigilance and drug safety processes
- Knowledge of healthcare terminology and clinical research concepts
- Familiarity with ICH guidelines and regulatory requirements
- Strong analytical and problem-solving skills
- Good communication and documentation abilities
- Proficiency in MS Office and basic computer applications
Experience
- Freshers can apply
- Candidates with prior healthcare or pharmacovigilance exposure will have an advantage
Location & Salary
- Job Locations: Hyderabad, Bengaluru, Mohali (India)
- Salary: As per industry standards for entry-level clinical research and pharmacovigilance roles
Application Process
Interested candidates can apply directly through the official Parexel careers portal using the link below:
Apply Here: https://jobs.parexel.com/en/job/-/-/877/92294780240
Why This Role Matters in Healthcare
This role plays a critical part in ensuring patient safety by monitoring adverse drug reactions and maintaining compliance with global regulatory standards. Pharmacovigilance professionals contribute directly to safer medicines, improved healthcare outcomes, and regulatory transparency across international markets.
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with Life Sciences, Pharmacy, Biotechnology, Microbiology, or related degrees can apply. Freshers are eligible.
2. Is prior experience required?
No. This role is suitable for freshers, though basic knowledge of pharmacovigilance is beneficial.
3. What is the career scope after this role?
You can grow into roles such as Drug Safety Associate, Pharmacovigilance Specialist, Clinical Research Associate, or Regulatory Affairs professional.
4. What skills are important for selection?
Strong attention to detail, analytical thinking, communication skills, and basic knowledge of drug safety processes.
5. Is this a good entry-level pharma job?
Yes. It is one of the best entry-level opportunities in clinical research and pharmacovigilance with a globally recognized CRO.
Summary Table
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Patient Safety Associate I |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Nursing |
| Experience | Freshers Eligible |
To apply for this job please visit jobs.parexel.com.
