Amaris Clinical Medical Writer Job 2026 | Clinical Research Career Opportunity (Amaris Clinical Medical Writer Job 2026) Introduction If you are looking to build a strong career in clinical research, medical writing, and regulatory documentation, then this opportunity can be a game-changer in 2026. Amaris Clinical is currently hiring skilled professionals for the Clinical Medical Writer position in India. This role is ideal for pharmacy graduates who want to work in clinical trials, BA/BE studies, and regulatory submissions. With growing demand in clinical research and global regulatory compliance, this job offers excellent career growth, industry exposure, and long-term stability. About The Company Amaris Clinical is an emerging clinical research and medical writing organization focused on delivering high-quality documentation, regulatory support, and clinical trial services. The company works in alignment with international regulatory standards such as ICH-GCP to ensure compli...
Get link
Facebook
X
Pinterest
Email
Other Apps
Pharma Duniya is a trusted platform providing the latest pharma job updates, walk-in interviews, clinical research openings, and pharmacy career guidance.
All job information is collected from official company websites and public sources.
We do not charge any fees and are not official recruiters.
Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Jobs for Freshers
Get link
Facebook
X
Pinterest
Email
Other Apps
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.
📄Resume Getting Rejected Again & Again?
👉 Not getting interview calls?
Most pharmaceutical job applications fail due to poorly formatted or non-ATS-friendly resumes.
👉 Get your Pharma Resume professionally written by experts:
Recommended Pharma Career & Job Updates (Must Read)
If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya 👇
"Regulatory Affairs Manager Job in Hyderabad 2026 – EU Markets | Masuu Global Pharma Jobs 💜🔥"
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences
📢 Stay Updated with Latest Pharma Jobs & Walk-In Interviews
If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.
✅ Join our WhatsApp Group ✅ Join our Telegram Channel
📌 Get verified pharma job alerts, interview tips, resume guidance, and student career support directly on your phone.
Aarogya Aadhar Healthcare Intern Work From Home 2026 | ABDM Digital Health Internship (Aarogya Aadhar Healthcare Intern Work From Home 2026) Introduction India’s digital health transformation is accelerating rapidly under government-led healthcare technology initiatives. The Aarogya Aadhar – One Nation One Health Card Project has announced an exciting Healthcare Intern (Work From Home) opportunity for 2026. This internship is specially designed for healthcare graduates who want to gain practical exposure in digital health records, healthcare IT systems, ABDM integration workflows, and public health digital infrastructure. If you are searching for a Healthcare Internship Work From Home India opportunity, this program can significantly strengthen your profile in healthcare IT, hospital administration, health informatics, and public health management. About The Organization – Aarogya Aadhar Aarogya Aadhar is a digital healthcare initiative aligned with the Government of India’s Ayu...
Mankind Pharma Walk-in Drive 2026 | QA, QC & Production Jobs in Udaipur & Behror (Mankind Pharma Walk-in Interview 2026) INTRODUCTION India ki top pharmaceutical companies me se ek Mankind Pharma ne 2026 ke liye ek badi Walk-in Interview Drive announce ki hai. Yeh hiring drive un candidates ke liye ek golden opportunity hai jo Quality Assurance (QA), Quality Control (QC), aur Production departments me apna career banana chahte hain. Agar aap pharma ya chemistry background se aate hain aur GMP environment, API ya formulation units me kaam kar chuke hain, to yeh walk-in interview aapke liye perfect ho sakta hai. Mankind Pharma apne Udaipur aur Behror (Rajasthan) manufacturing plants ke liye experienced professionals ko hire kar rahi hai, jiska interview Indore location par conduct hoga. ABOUT THE COMPANY – MANKIND PHARMA Mankind Pharma Limited India ki fastest growing pharmaceutical company me se ek hai. Company ki shuruaat 1995 me hui thi aur aaj yeh comp...
Global Pharma Hiring 30 Drug Safety Trainee in Bangalore 2026 | Pharmacovigilance Jobs for Freshers (Global Pharma Hiring 30 Drug Safety Trainees) INTRODUCTION Pharmacovigilance industry India me tezi se grow kar rahi hai aur 2026 me Drug Safety freshers ke liye bahut achhe career opportunities open ho rahe hain. Ek reputed Global Pharmaceutical Company ne Bangalore location ke liye 30 Drug Safety Trainee positions announce ki hain. Yeh role un candidates ke liye best hai jo Pharmacovigilance, Adverse Event Processing, aur Clinical Safety me apna career start karna chahte hain. Agar aap B.Pharm, M.Pharm, PharmD ya MSc Life Sciences background se ho aur Drug Safety me entry lena chahte ho to yeh opportunity aapke liye perfect starting point ho sakti hai. Company proper training, global exposure aur long-term career growth provide karegi. ABOUT THE COMPANY Hiring company ek globally recognised pharmaceutical organisation hai jo Drug Safety, Clinical Research, aur Pharmacovigilanc...
IKS Health Walk-In Interview for B.Pharm Freshers – Swift Scribing Job in Navi Mumbai (IKS Health Walk-In Interview for B.Pharm Freshers) If you are a B.Pharmacy fresher searching for healthcare IT jobs in Mumbai, this is an excellent opportunity to begin your corporate career. IKS Health is conducting a walk-in interview for the position of Swift Scribing at its Navi Mumbai office. This job is especially suitable for pharmacy freshers who want to build a career in medical documentation, clinical support services, and healthcare operations. With the rapid digital transformation in global healthcare systems, medical scribing and electronic health record (EHR) documentation roles are in high demand. For B.Pharm graduates, this position offers structured working hours, corporate exposure, and international healthcare process experience. Introduction (Overview of the Opportunity) Healthcare documentation and medical scribing jobs are becoming popular career options for life sciences...
IQVIA Hiring Clinical Research Associate ( CRA 2) in Thane – Pharma Job Opportunity 2026 IQVIA Hiring Clinical Research Associate (CRA 2) Introduction The clinical research industry is rapidly expanding worldwide , creating new opportunities for professionals with backgrounds in pharmacy, life sciences, and healthcare. Contract Research Organizations ( CROs) play a critical role in managing clinical trials and supporting pharmaceutical companies in drug development. One of the leading global CRO companies, IQVIA, has announced a new job opening for a Clinical Research Associate (CRA 2) position in Thane, Maharashtra, India. This role is ideal for professionals who have experience in clinical trial monitoring and a strong understanding of regulatory guidelines such as ICH- GCP. The CRA 2 position involves monitoring clinical trial sites, ensuring compliance with protocols, and maintaining data integrity throughout the study process. Candidates selected for this role will work close...
"Regulatory Affairs vs Pharmacovigilance vs QA – Which Career Is Best in 2026 ?" (Regulatory Affairs vs Pharmacovigilance vs QA - Which Career Is Best?) In today’s fast-growing pharmaceutical industry, choosing the right career path is one of the most crucial decisions for science and pharmacy graduates. Among the top career domains — Regulatory Affairs (RA), Pharmacovigilance (PV), and Quality Assurance (QA) — each plays a vital role in ensuring that medicines are safe, effective, and compliant with global standards. But the real question is — which field is the best to build a future-proof career in 2025 and beyond? Let’s dive deep into the comparison of these three key pharma domains based on skills, job opportunities, salaries, and growth prospects. Understanding the Three Career Paths:- Regulatory Affairs (RA): Regulatory Affairs professionals act as the bridge between pharmaceutical companies and government regulatory agencies (like CDSCO, USFDA, EMA, etc.). Their main ...
Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya. (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. ELEXES ...
Share on WhatsApp
