Latest pharma jobs Clinical Operations Associate Parexel job for freshers and experienced candidates apply online eligibility salary details
Introduction
If you are looking to enter or grow in the clinical research field, this opportunity can be a great career move. The Clinical Operations Associate Parexel Job 2026 offers hands-on experience in clinical trial coordination, site management, and documentation. This role is ideal for candidates who want to work closely with clinical teams and contribute to the successful execution of global clinical studies.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Operations Associate |
| Company Name | Parexel |
| Location | Bengaluru, India |
| Employment Type | Full-Time |
| Department | Clinical Operations / Clinical Research |
| Experience Required | Preferred (Entry-Level to Experienced) |
| Education | Life Science Degree / Relevant Qualification |
| Salary | As per company norms |
Company Overview
Parexel is a globally recognized contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies across the entire clinical development lifecycle. The company is known for its patient-centric approach and its commitment to delivering high-quality clinical research solutions.
At Parexel, employees work on projects that directly contribute to the development of life-saving therapies, making it a meaningful and impactful workplace.
Job Location & Employment Type
This role is based in Bengaluru, India, and is a full-time position. Candidates will work in a structured clinical operations environment supporting global trials.
Open Positions / Department Details
The position is part of the Clinical Operations team, responsible for supporting clinical trials from initiation to closure.
Key functional areas include:
- Clinical trial coordination
- Site management support
- Trial Master File (TMF) handling
- Clinical documentation and tracking
Key Roles & Responsibilities
As part of the Clinical Operations Associate Parexel Job, your responsibilities will include:
Project Initiation & Planning
- Supporting site activation activities and system access setup
- Coordinating training completion for site staff
- Managing shipment of study materials and documents
- Assisting in preparation of Investigator Site Files
Project Maintenance
- Managing and updating Trial Master File (TMF) documents
- Following up with sites for pending documents and actions
- Supporting clinical project teams with data and updates
- Assisting in payment processes and resolving site issues
- Updating clinical systems like CTMS and trackers
Project Close-Out
- Coordinating return of equipment and materials
- Assisting with database lock activities
- Supporting completion of site closeout procedures
Operational Responsibilities
- Ensuring compliance with ICH-GCP guidelines and regulatory requirements
- Completing administrative tasks such as reports and training
- Identifying potential issues and escalating when needed
- Supporting continuous improvement and team collaboration
Eligibility Criteria
Education
- Degree in:
- Life Sciences
- Pharmacy
- Biotechnology
- Related field
- Diploma or equivalent experience may also be considered
Experience
- Clinical research experience preferred, such as:
- Clinical Trial Assistant (CTA)
- Study Coordinator
- Site Management roles
Skills Required
- Knowledge of clinical trial processes and documentation
- Familiarity with CTMS, EDMS, and EDC systems
- Strong MS Office skills (Excel, Word, PowerPoint)
- Good communication and organizational skills
- Ability to manage multiple tasks and deadlines
- Attention to detail and problem-solving ability
- Teamwork and proactive mindset
Salary & Benefits
Salary: As per company norms
Benefits include:
- Opportunity to work on global clinical trials
- Career growth in clinical operations
- Learning and development opportunities
- Exposure to regulatory processes and systems
- Professional and collaborative work environment
Selection Process
The hiring process for the Clinical Operations Associate Parexel Job typically includes:
- Resume screening
- Technical/functional interview
- HR discussion
- Final selection
How to Apply
Candidates can apply through the online application process:
- Visit the official careers page of Parexel
- Search for Job ID: R0000040831
- Fill out the application form
- Upload your resume
- Submit your application
Apply as soon as possible due to limited application time.
Important Dates
- Last Date to Apply: April 27, 2026
Why Apply for This Job?
The Clinical Operations Associate Parexel Job 2026 offers strong benefits for career growth:
- Entry into global clinical research operations
- Hands-on experience in trial coordination and site management
- Exposure to international regulatory standards
- Opportunity to work with experienced clinical teams
- Strong career path in clinical operations and project management
- Work with a reputed CRO organization
This role is ideal for candidates aiming to build a career in clinical operations, clinical research, or regulatory affairs.
FAQs
1. What is the focus keyword for this job?
The focus keyword is Clinical Operations Associate Parexel Job.
2. Is this job suitable for freshers?
Freshers with relevant education can apply, but prior clinical research experience is preferred.
3. What is the last date to apply?
The last date is April 27, 2026.
4. What is the job location?
The position is based in Bengaluru, India.
5. What systems should candidates be familiar with?
Knowledge of CTMS, EDMS, and MS Office tools is important.
Conclusion
The Clinical Operations Associate Parexel Job 2026 is an excellent opportunity for candidates seeking to establish a career in clinical research. With exposure to global trials, regulatory compliance, and hands-on operational work, this role provides a strong foundation for long-term growth. Interested candidates should apply online before the deadline.
Disclaimer
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