Parexel Hiring Clinical Operations Assistant
- Parexel Hiring Clinical Operations Assistant in Mumbai | Clinical Trials Jobs for Freshers & Experienced
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What does a Clinical Operations Assistant do?
- Is prior clinical trial experience mandatory?
- What systems should candidates know?
- What is the work location?
Parexel Hiring Clinical Operations Assistant in Mumbai | Clinical Trials Jobs for Freshers & Experienced
Looking to build a career in clinical research and clinical trials operations? Parexel is hiring for the role of Clinical Operations Assistant in Mumbai. This opportunity is ideal for life science graduates and candidates with clinical research exposure who want to work in global clinical trials and regulatory-compliant environments.
This role offers strong career growth in clinical operations, site management, and trial coordination, making it a valuable entry point into the CRO industry.
Company Overview
Parexel is a leading global Clinical Research Organization (CRO) that provides clinical development, regulatory consulting, and market access solutions to pharmaceutical and biotechnology companies worldwide. With a strong presence in clinical trials and drug development, Parexel plays a critical role in bringing life-saving therapies to patients faster.
The company is known for its high standards in ICH-GCP compliance, quality-driven processes, and patient-focused research, making it one of the most trusted names in the clinical research industry.
Job Role & Responsibilities
As a Clinical Operations Assistant, you will support clinical trial activities and ensure smooth coordination between study teams, sites, and internal stakeholders.
Key Responsibilities:
Project Initiation & Planning
- Support site activation activities and system access setup
- Coordinate training completion for site staff and vendor systems
- Assist in preparation and shipment of Investigator Site Files
- Coordinate shipment of study materials and equipment
Project Maintenance
- Maintain and update Trial Master File (TMF) ensuring inspection readiness
- Follow up with sites and internal teams for pending documents and actions
- Support Electronic Data Capture (EDC) updates and documentation
- Assist in investigator payment tracking and site issue resolution
- Contribute to Clinical Trial Management System (CTMS) updates and tracking
Project Close-Out
- Coordinate return of equipment and materials
- Support database lock activities
- Ensure completion of site close-out documentation and procedures
Operational Responsibilities
- Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
- Manage administrative tasks, training, and documentation
- Identify and escalate issues proactively
- Collaborate with CRAs and clinical teams for smooth trial execution
This role plays a critical part in maintaining data integrity, regulatory compliance, and operational efficiency in clinical trials.
Eligibility / Qualifications
Educational Qualification:
B.Pharm, M.Pharm, BSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing, Pharmacy, Clinical Research or related fields
Experience:
- Freshers with relevant knowledge can apply
- Prior experience in clinical research (CTA, CRC, etc.) preferred
Skills Required:
- Knowledge of clinical trials and ICH-GCP guidelines
- Familiarity with CTMS, EDC, and TMF systems (preferred)
- Strong organizational and multitasking skills
- Good communication and documentation skills
- Attention to detail and problem-solving ability
Location & Salary
- Location: Mumbai, India
- Work Mode: Office-based
- Salary: Not disclosed (competitive as per CRO industry standards)
Application Process
Interested candidates can apply online through the official Parexel careers page:
Apply Here: https://jobs.parexel.com/en/job/-/-/877/93975925184?
Ensure your resume highlights clinical research knowledge, documentation skills, and any experience with clinical trial processes.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes, freshers with life science background and clinical research knowledge can apply.
What does a Clinical Operations Assistant do?
They support clinical trial activities, documentation, and site coordination.
Is prior clinical trial experience mandatory?
No, but it is preferred and gives an advantage.
What systems should candidates know?
CTMS, EDC, and TMF systems knowledge is beneficial.
What is the work location?
Mumbai, India.
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Clinical Operations Assistant |
| Required Education | B.Pharm, M.Pharm, BSc, Biotechnology, Nursing, Clinical Research |
| Experience | Freshers / Experienced |
To apply for this job please visit jobs.parexel.com.
