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Parexel Hiring For Clinical Operations Assistant

Published on

Bachelor’s degree in Life Sciences, Pharmacy, Nursing

Bengaluru, India

1–2 years

Verified Job

Online Application

Position: Clinical Operations Assistant
Location: Bengaluru, India
Employment Type: Full-time
Experience Required: 1–2 years


Job Description

About Parexel

Parexel International is a leading global Clinical Research Organization (CRO) that supports pharmaceutical, biotechnology, and medical device innovations. With a strong presence in over 100 countries, Parexel is known for its cutting-edge clinical trials, regulatory consulting, and patient-centric research solutions.

Joining Parexel means being part of a dynamic team that accelerates drug development and improves patient outcomes worldwide.

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Key Responsibilities

1. Central File & Documentation Management

  • Track, scan, label, and upload clinical documents to Central File (CF) and Work In Progress (WIP) systems.
  • Archive wet-ink documents following the Central File Maintenance Plan (CFMP).
  • Conduct quality checks to ensure compliance with SOPs and regulatory standards.
  • Handle photocopying, printing, and document retrieval as needed.

2. Clinical Trial Support & Tracking

  • Maintain study-specific trackers and Clinical Trial Management Systems (CTMS).
  • Monitor reporting timelines for regulatory submissions and site safety updates.
  • Assist with translation workflows and approvals via platforms like Oracle.

3. Administrative & Site Coordination

  • Manage courier shipments, signature collections, and invoice processing.
  • Support Japanese clinical sites with document coordination.

Eligibility Criteria

Educational Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related healthcare fields.
  • Equivalent nursing or clinical research certifications are also acceptable.

Skills & Experience

  • 1–2 years of experience in clinical research, CROs, or pharma/biotech.
  • Familiarity with CTMS, Impact Harmony, and eTMF systems.
  • Strong organizational, communication, and time-management skills.
  • Knowledge of ICH-GCP, regulatory documentation, and clinical trial protocols.

Why Join Parexel?

✅ Global Exposure – Work on international clinical trials with top pharmaceutical companies.
✅ Career Growth – Access to APEX program for fast-tracked promotions into clinical roles.
✅ Learning & Development – Structured training in clinical operations and regulatory compliance.
✅ Work-Life Balance – Supportive work culture with flexible policies.


Application Link

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