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Cliantha Research Hiring: Report Writer & QC Reviewer – Apply Now!

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Cliantha Research

0 - 2 Years

3 - 3.5 LPA

Gujarat

B.Sc / B.Pharma / M.Sc / M.Pharma

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Job highlights

Work/Life Balance

Time management

challenging projects

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Are you looking for exciting career opportunities in clinical research? Cliantha Research, a leading contract research organization (CRO), is hiring for Report Writer (Ahmedabad) and QC Reviewer (Vadodara) positions. If you have a background in clinical research, pharmaceuticals, or life sciences, this could be your next career move!

Job Openings at Cliantha Research

1. Report Writer – Ahmedabad

Experience: 1-2 Years
Salary: ₹2.5-3.5 LPA
Qualifications: M.Sc / M.Pharma

Job Description:

  • Generate Clinical Study Reports (CSR) as per ICH E3 guidelines, protocol, and regulatory requirements.
  • Train new employees in report writing and ensure timely completion of tasks.
  • Prepare and update in-house clinical report templates.
  • Handle sponsor and regulatory queries related to clinical reports.
  • Review and update Clinical Report SOPs for compliance.

Key Skills: Report Writing, ICH Guidelines, Clinical Data Review, SOP Compliance


2. QC Reviewer – Vadodara

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Experience: 0-1 Year
Salary: ₹2-3 LPA
Qualifications: B.Sc / B.Pharma / M.Sc / M.Pharma

Job Description:

  • Review clinical raw data for accuracy, completeness, and compliance with GCP, SOPs, and study protocols.
  • Conduct online monitoring of study activities to ensure regulatory adherence.
  • Manage issuance and reconciliation of controlled documents.
  • Assist in QA audits, archiving, and source data verification (SDV).
  • Review safety lab data and tabular listings in clinical reports.

Key Skills: Quality Control, GCP Compliance, Data Review, Clinical Research


About Cliantha Research

Cliantha Research is a globally recognized Contract Research Organization (CRO) offering end-to-end clinical research services. With a strong presence in Ahmedabad, Vadodara, and international locations, Cliantha specializes in bioanalytical, clinical, and regulatory research. The company is known for its high-quality compliance with ICH-GCP, FDA, and EMA guidelines, making it a trusted partner for pharmaceutical and biotech firms.

Why Join Cliantha Research?

✅ Industry-leading training & career growth
✅ Work on global clinical trials
✅ Competitive salary & benefits
✅ Employee-friendly work culture


How to Apply?

🔗 Apply for Report Writer (Ahmedabad) – Click Here
🔗 Apply for QC Reviewer (Vadodara) – Click Here

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