Cliantha Hiring QA Auditor, Medical Monitor, Biometrics

BPharm MSc Clinical Jobs Cliantha Ahmedabad Hiring

Cliantha hiring QA Auditor, Medical Monitor, Biometrics roles in Ahmedabad. BPharm, MSc, MBBS eligible. Multiple vacancies.

Cliantha Research is actively hiring for multiple vacancies across Quality Assurance, Clinical Research, Biometrics, Medical Affairs, and Business Development departments at its Ahmedabad location. The company is offering diverse roles including QA Auditor (Lab), Trainer, Global Compliance Cell Auditor, Report Writer (Biometrics), Medical Monitor, Business Development (Consumer Research), and Proposal Developer (Late Phase).

This hiring drive is open for both freshers and experienced professionals, with experience requirements ranging from 0 to 10 years depending on the role. Candidates from pharmacy, life sciences, clinical research, and medical backgrounds will find this opportunity highly aligned with careers in clinical trials, regulatory compliance, pharmacovigilance, and healthcare analytics.

Company Overview

Cliantha Research is a globally recognized clinical research organization (CRO) with operations across India, USA, and Canada. The company specializes in clinical trials, bioanalytical services, and regulatory support for pharmaceutical, biotechnology, and medical device companies.

With a strong focus on Good Clinical Practice (GCP), regulatory compliance, and data integrity, Cliantha Research plays a key role in accelerating drug development and ensuring patient safety. The organization is known for its scientific expertise, ethical standards, and commitment to delivering high-quality clinical research services.

Working at Cliantha offers professionals exposure to global clinical trials, regulatory frameworks, and advanced biometrics and data analysis systems.

Job Role & Responsibilities

QA Auditor – Laboratory

• Conduct internal audits for laboratory operations and quality systems
• Ensure compliance with GLP, GCP, and regulatory standards
• Identify gaps and support corrective and preventive actions (CAPA)
• Maintain audit documentation and compliance reports

Trainer (Clinical & QA Training)

• Deliver training programs on GCP, SOPs, and regulatory guidelines
• Develop training materials and learning modules
• Assess training effectiveness and employee competency

Global Compliance Cell Auditor

• Perform audits aligned with global GCP standards
• Review clinical trial processes and documentation
• Support regulatory inspections and compliance strategies

Report Writer – Biometrics

• Prepare clinical study reports and statistical summaries
• Work with clinical data, analysis outputs, and reporting tools
• Ensure accuracy and compliance with regulatory submission standards

Medical Monitor

• Provide medical oversight for clinical trials
• Review safety data and patient outcomes
• Support protocol development and clinical decision-making

Business Development – Consumer Research

• Conduct market research and analyze healthcare trends
• Support client acquisition and business growth strategies
• Collaborate with cross-functional teams for project proposals

Proposal Developer – Late Phase

• Prepare proposals for clinical trials and late-phase studies
• Conduct literature research and cost analysis
• Support bid defense and client communication

Eligibility / Qualifications

Candidates must have completed:

B.Pharm, M.Pharm, M.Sc, Pharm.D, MBBS + MD Pharmacology

Relevant courses include: Clinical Research, Pharmacology, Biostatistics, Biotechnology, Healthcare Management, Drug Regulatory Affairs, Medical Writing, Data Analysis

• Experience: 0 to 10 years depending on role
• Strong understanding of GCP, GLP, and clinical trial processes preferred
• Experience in CRO, clinical research, or regulatory environments is an advantage
• Good communication, analytical, and documentation skills required

Location & Salary

• Job Location: Ahmedabad
• Salary: Competitive and based on role, qualification, and experience

Application Process

Interested candidates can apply by sending their updated resume to:

• vdesai@cliantha.com
• mjunnarkar@cliantha.com

For more information, visit:
https://www.cliantha.com

Ensure your resume highlights your experience in clinical research, QA auditing, biometrics, or healthcare roles to improve your chances of selection.

Why This Opportunity Stands Out

• Work with a global clinical research organization (CRO)
• Opportunities across QA, clinical trials, biometrics, and medical roles
• Exposure to GCP, regulatory compliance, and global clinical studies
• Career growth in clinical research, pharmacovigilance, and healthcare analytics
• Opportunity to contribute to drug development and patient safety

FAQs

Who can apply for these roles?
Candidates with pharmacy, life sciences, or medical qualifications can apply.

Are freshers eligible?
Yes, freshers can apply for select roles like Medical Monitor and Report Writer.

What is the experience requirement?
0 to 10 years depending on the role.

What areas are covered in these roles?
Clinical trials, QA auditing, biometrics, medical monitoring, and business development.

How to apply?
Send your updated resume to the provided email IDs.

Summary Table

Category	Details
Company	Cliantha Research
Vacancies	QA Auditor, Medical Monitor, Biometrics Report Writer, Trainer, BD Executive
Required Education	B.Pharm, M.Pharm, M.Sc, Pharm.D, MBBS + MD
Experience	0 to 10 Years