PharmaZones Hiring Clinical Research Associate (CRA)
- PharmaZones Hiring Clinical Research Associate (CRA) – 1–2 Year Experience Jobs in Ahmedabad
- Company Overview
- Job Role & Responsibilities
- Clinical Research Associate (CRA)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What does a CRA do?
- Is travel required?
- What career growth can I expect?
- Summary
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.
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.
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
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
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.
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.
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.
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) |
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