Advanced Clinical Hiring Senior & Principal Clinical Data Associates in Ahmedabad | Clinical Data Management Jobs 2026 (Advanced Clinical Hiring Senior & Principal Clinical Data Associates in Ahmedabad) Introduction The demand for skilled Clinical Data Management professionals in India is increasing rapidly as pharmaceutical companies and Contract Research Organizations (CROs) continue expanding their global clinical trial operations. Advanced Clinical, a globally recognized clinical development and strategic resourcing company, has announced exciting career opportunities for experienced Clinical Data Management professionals in Ahmedabad, Gujarat. The company is currently hiring for: Senior Clinical Data Associate Principal Clinical Data Associate These Clinical Data Management jobs in Ahmedabad are ideal for professionals with experience in: Clinical trial data review EDC systems SAE reconciliation eCRF review CDASH standards CRO and pharmaceutical environments Candida...
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Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Jobs for Freshers
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Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Career Opportunity
(Parexel Hiring Patient Safety Associate I in Mohali)
Introduction
If you are looking to start your career in pharmacovigilance and drug safety, this opportunity from Parexel is highly valuable. The company is hiring for the role of Patient Safety Associate I in Mohali, India, which is ideal for freshers and early-career professionals in pharmacy and life sciences.
With the growing demand for drug safety professionals in 2026, roles like Patient Safety Associate are becoming one of the best entry points into the clinical research and pharmacovigilance industry. This job provides hands-on experience in ICSR processing, MedDRA coding, safety reporting, and global regulatory compliance.
About The Company
Parexel is a globally recognized Contract Research Organization (CRO) that provides clinical research, consulting, and regulatory services to pharmaceutical, biotechnology, and medical device companies.
Founded: 1982 Headquarters: Durham, North Carolina, USA Industry: Clinical Research / CRO Employees: 20,000+ worldwide
Parexel operates in more than 100 countries and plays a key role in supporting clinical trials, drug development, and regulatory approvals globally. The company is known for its strong focus on patient safety, regulatory excellence, and innovation in healthcare.
Job Overview Summary
The Patient Safety Associate I role at Parexel focuses on pharmacovigilance operations, including ICSR processing, safety data management, and regulatory reporting.
This position is ideal for candidates who want to build expertise in drug safety, adverse event reporting, and clinical research processes. You will work closely with global teams and regulatory authorities to ensure compliance and patient safety.
Vacancy Details
Company: Parexel Job Role: Patient Safety Associate I Location: Mohali, India Job Type: Full-Time Industry: Pharmacovigilance / Clinical Research Experience: Freshers or early-career candidates
Responsibility Explanation
In this role, you will be involved in multiple pharmacovigilance and safety-related activities. Your primary work will include processing Individual Case Safety Reports (ICSRs), ensuring data accuracy, and maintaining compliance with global regulatory standards.
You will monitor safety reports from various sources, including literature, EudraVigilance, and internal databases. The job also involves MedDRA coding, preparing adverse drug reaction (ADR) narratives, and performing quality checks on safety data.
Additionally, you will support regulatory submissions, maintain audit documentation, and collaborate with global teams. Literature review and signal detection are also part of the role, where you identify potential safety concerns related to drugs.
Freshers or candidates with basic pharmacovigilance exposure can apply
Skills Required
To succeed in this pharmacovigilance role, candidates must develop both technical and soft skills.
Key skills include strong knowledge of pharmacovigilance concepts, ICH guidelines, and ICSR workflow. Understanding of drug safety databases and MedDRA coding is an added advantage.
Candidates should also have good communication skills, analytical thinking, and attention to detail. Basic knowledge of Microsoft Office tools is essential for documentation and reporting.
Salary Estimate
The estimated salary for this role is between ₹3.5 LPA and ₹6 LPA, depending on skills and performance.
Freshers usually start at the lower range, but with experience in pharmacovigilance, salary growth is fast. Within 2–3 years, professionals can move to higher roles with better packages.
Interview Details: The interview process may include:
HR Interview Technical Interview (Pharmacovigilance basics, ICSR, ADR) Communication and Analytical Assessment
Shortlisted candidates will be contacted by the company after application review.
Required Documents
Candidates should prepare the following documents before applying:
Make sure to apply as soon as possible, as positions may close once filled.
FAQs
What is the role of a Patient Safety Associate?
A Patient Safety Associate works in pharmacovigilance to monitor drug safety, process ICSRs, and ensure regulatory compliance.
Can freshers apply for Parexel jobs?
Yes, freshers with a pharmacy or life sciences background can apply for this role.
What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report, which contains information about adverse drug reactions.
Is pharmacovigilance a good career in 2026?
Yes, pharmacovigilance is one of the fastest-growing career fields with high demand globally.
Final Conclusion
The Patient Safety Associate I role at Parexel is a great opportunity for freshers and early-career professionals to enter the pharmacovigilance industry. With strong training, global exposure, and career growth, this job can help you build a successful career in drug safety and clinical research.
If you are serious about working in pharma jobs related to safety, regulatory compliance, and clinical trials, this is the right time to start. Focus on building your skills, apply consistently, and stay updated with industry trends.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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