PharmaZones Hiring Clinical Research Associate (CRA)

PharmaZones Hiring Clinical Research Associate (CRA) – 1–2 Year Experience Jobs in Ahmedabad

PharmaZones is hiring Clinical Research Associate (CRA) professionals in Ahmedabad for roles within the GCP (Good Clinical Practice) department. This is a full-time opportunity for candidates with 1–2 years of experience in clinical research, particularly in monitoring clinical trials and bioequivalence studies.

Multiple openings are expected for this CRA role, making it a strong opportunity for candidates with prior CRC or CRA experience who want to transition into advanced clinical monitoring and site management roles.

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Company Overview

PharmaZones is a clinical research-focused organization involved in managing clinical trials, bioequivalence studies, and regulatory-compliant research activities. The company collaborates with sponsors, CROs, and research sites to ensure high-quality study execution aligned with global standards.

With a growing presence in clinical operations, PharmaZones provides professionals with hands-on exposure to monitoring, regulatory compliance, and trial lifecycle management.

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Job Role & Responsibilities

Clinical Research Associate (CRA)

• Monitor Phase clinical trials and bioequivalence studies at investigator sites
• Conduct site feasibility, qualification, initiation, monitoring, and close-out visits
• Ensure compliance with ICH-GCP guidelines and study protocols
• Prepare monitoring visit reports and maintain accurate study documentation
• Apply risk-based monitoring strategies to improve study efficiency
• Coordinate with sites, CROs, and internal teams for smooth study execution
• Track study progress and ensure timelines are met
• Identify issues and implement corrective actions proactively
• Handle Adverse Event (AE) and Serious Adverse Event (SAE) reporting
• Collaborate with project managers and stakeholders for project deliverables

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Eligibility / Qualifications

• Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research)
• Experience: 1–2 years as CRA or Clinical Research Coordinator (CRC)
• Strong knowledge of clinical trial processes and GCP guidelines
• Good communication, coordination, and problem-solving skills
• Willingness to travel for site monitoring visits

Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research

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Location & Salary

• Job Location: Ahmedabad, Gujarat, India
• Work Mode: On-site with travel requirements
• Salary Range: ₹4.5 LPA – ₹8.5 LPA (approximate based on CRA experience and industry standards)

This role offers strong growth potential in clinical operations and monitoring roles.

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Application Process

Interested candidates can apply by sending their updated CV:

Email: hr@pharmazones.com
Contact: 9898778211

Shortlisted candidates will be contacted for further selection rounds.

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Frequently Asked Questions (FAQs)

Is this role suitable for freshers?

No, this role requires 1–2 years of clinical research experience.

What does a CRA do?

A CRA monitors clinical trials, ensures protocol compliance, and manages site activities.

Is travel required?

Yes, frequent travel is required for site monitoring visits.

What career growth can I expect?

You can grow into Senior CRA, Clinical Project Manager, or Clinical Operations roles.

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Summary

Category	Details
Company	PharmaZones
Vacancies	Clinical Research Associate (CRA)
Required Education	B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research)
Experience	1–2 years (CRA/CRC experience)

Tagged as: Pharma Jobs in Ahmedabad