Looking for Clinical Quality Assurance (QA) jobs in pharma or CRO industry?
Synergen Bio is hiring Research Associate-I (Clinical QA) for experienced professionals in clinical research compliance and audits.
This is a great opportunity for candidates with 3+ years of experience in Clinical QA who want to work in a quality-driven clinical research environment.
Job Overview
- Company: Synergen Bio
- Role: Research Associate-I
- Department: Clinical Quality Assurance
- Experience: 3+ Years
- Qualification: B.Pharm / M.Pharm
- Vacancies: 02
- Work Type: On-site
About Synergen Bio
Synergen Bio is a specialized Clinical Research Organization (CRO) focused on:
- Bioanalytical services
- Clinical study management
- Regulatory compliance
The company is known for its strong quality systems, global regulatory standards, and scientific excellence in clinical research.
Job Role – Research Associate-I (Clinical QA)
This role plays a key part in maintaining GCP compliance, audit processes, and quality systems in clinical studies.
Eligibility Criteria
- B.Pharm or M.Pharm graduates
- Minimum 3+ years of experience in Clinical QA
- Experience in CRO/clinical research environment preferred
- Immediate joiners will be given preference
Skills Required
- Strong knowledge of GCP guidelines & SOPs
- Experience in clinical audits & QA systems
- Good documentation and reporting skills
- Attention to detail and compliance mindset
- Ability to work independently
Key Responsibilities
- Conduct in-process and retrospective audits
- Review raw data and clinical study reports
- Implement CAPA (Corrective & Preventive Actions)
- Report audit findings to QA leadership
- Provide training on GCP and regulatory guidelines
- Prepare and review SOPs
- Perform vendor, facility, and system audits
- Handle deviations and trend analysis
- Maintain documentation and audit records
- Verify calibration and validation documentation
Benefits & Perks
- Career growth in Clinical QA domain
- Exposure to global regulatory standards
- Learning opportunities in advanced QA systems
- Collaborative and professional work environment
- Long-term stability in CRO industry
How to Apply
Interested candidates should send their updated CV to:
👉 Mention “Research Associate-I – Clinical Quality Assurance” in the subject line.
👉 Immediate joiners are preferred.
Why You Should Join Synergen Bio
- Work in a quality-focused CRO environment
- Gain expertise in clinical audits & regulatory compliance
- Be part of global clinical research processes
- Strong career progression in QA field
FAQs
1. What experience is required?
Minimum 3+ years in Clinical Quality Assurance.
2. What qualifications are needed?
B.Pharm or M.Pharm.
3. Is this a walk-in job?
No, application is via email only.
4. How many vacancies are available?
There are 2 openings.
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