Parexel Hiring 2026: Multiple Clinical Research, PV & Regulatory Jobs | Freshers & Experienced Apply
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(Parexel Hiring 2026: Multiple Clinical Research, PV & Regulatory Jobs) |
Introduction
If you are searching for high-growth pharma jobs in India, this latest hiring update from Parexel can be a game-changing opportunity. Parexel, a globally recognized Contract Research Organization (CRO), is offering multiple job roles across clinical research, pharmacovigilance, regulatory affairs, and analytics domains.
This hiring drive is suitable for both freshers and experienced professionals who want to build a strong career in clinical trials, drug safety, and regulatory compliance. With remote and hybrid work options available, this opportunity aligns perfectly with the evolving pharma industry trends in 2026.
About The Company
Parexel is a leading global CRO headquartered in Durham, North Carolina, USA. Established in 1982, the company has grown into one of the most trusted names in clinical research and drug development services.
Parexel operates in over 100 countries and employs more than 21,000 professionals worldwide. The company provides services in clinical trials, regulatory consulting, pharmacovigilance, and data analytics, helping pharmaceutical and biotech companies bring new therapies to market faster and more efficiently.
Job Overview Summary
Parexel is currently hiring for multiple roles across India, including Hyderabad, Bengaluru (remote), and Mohali (remote). These roles cover various domains such as clinical operations, regulatory affairs, pharmacovigilance, and data analytics.
This hiring is ideal for candidates at different career stages, from entry-level freshers to highly experienced professionals, making it one of the most versatile pharma job opportunities in 2026.
Vacancy Details
Company: Parexel
Job Locations: Hyderabad, Bengaluru (Remote), Mohali (Remote)
Job Type: Full-Time
Experience: Freshers to 8+ Years
Open Positions:
Clinical Operations Associate (Entry-Level)
Senior Regulatory Affairs Associate
Senior Medical Device Documentation Associate
Senior Drug Safety Physician
Real-time Visual Analytics Specialist
Responsibility Explanation
In these roles, candidates will be involved in core pharmaceutical and clinical research activities. Responsibilities include managing clinical trials, ensuring regulatory compliance, performing pharmacovigilance activities, and handling data analytics.
Clinical roles will focus on trial coordination, TMF management, and site communication. Regulatory roles involve dossier preparation and global submissions. Pharmacovigilance roles require safety monitoring, signal detection, and medical review. Analytics roles focus on interpreting clinical data and generating insights using tools like R and dashboards.
Eligibility Criteria (Official)
Education:
B.Pharm / M.Pharm / PharmD / Life Sciences / MBBS (role-specific)
Experience:
Freshers to 8+ years, depending on role
Knowledge Required:
ICH-GCP guidelines
Clinical trials and pharmacovigilance processes
Regulatory frameworks
Skills Required
Candidates should have strong analytical thinking, communication skills, and the ability to work in a fast-paced environment. Knowledge of clinical documentation, regulatory submissions, and safety data handling is highly valuable.
For analytics roles, candidates must be comfortable with data visualization tools like R or Excel. Soft skills like teamwork, adaptability, and problem-solving are equally important for success in CRO environments.
Salary Estimate
Entry-Level Roles: ₹3.5 – ₹6 LPA
Mid-Level Roles: ₹6 – ₹12 LPA
Senior Roles: ₹18 – ₹35+ LPA
Salary depends on experience, domain expertise, and job role.
Interview Details (Official)
Interview Mode: Online / Virtual
Selection Process:
Resume Screening → Technical Interview → HR Discussion
Required Documents
Candidates should keep the following documents ready:
Updated Resume (CV)
Educational Certificates
Experience Letters (if applicable)
Government ID Proof (Aadhaar/PAN)
Passport Size Photographs
How to Apply
Candidates can apply through the official links below:
Clinical Operations Associate
Regulatory Affairs
Medical Device Documentation
Drug Safety Physician
Visual Analytics Specialist
FAQs Section
Q1. Can freshers apply for Parexel jobs?
Yes, freshers can apply for entry-level roles like Clinical Operations Associate.
Q2. What is the salary at Parexel India?
Salary ranges from ₹3.5 LPA to ₹35+ LPA depending on role and experience.
Q3. Is Parexel a good company for pharma careers?
Yes, Parexel is one of the top CROs globally, offering excellent career growth.
Q4. Are remote jobs available in Parexel?
Yes, several roles are available in remote or hybrid mode.
Final Conclusion
Parexel hiring 2026 offers one of the best opportunities for candidates aiming to build a career in clinical research, pharmacovigilance, and regulatory affairs. Whether you are a fresher or an experienced professional, this hiring drive provides multiple entry points into the global CRO industry.
With strong career growth, international exposure, and competitive salaries, Parexel stands out as a top choice for pharma professionals in India.
If you are serious about building a long-term career in pharma, clinical trials, or drug safety, applying to Parexel can be a smart and strategic move.
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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