Synergen Bio is hiring for Research Associate-I in Clinical Quality Assurance. This is a great pharma job opportunity for B.Pharm/M.Pharm professionals with 3+ years of experience in clinical QA. Immediate joiners preferred for this critical role in clinical research compliance.
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About the Company
Synergen Bio is a specialized clinical research organization (CRO) focused on delivering high-quality bioanalytical and clinical study services. The company is known for its strong emphasis on regulatory compliance, scientific excellence, and innovation in clinical trials. With a commitment to quality standards and global best practices, Synergen Bio supports pharmaceutical and biotech companies in bringing safe and effective therapies to market efficiently.
Job Details
- Company Name: Synergen Bio
- Experience: 3+ Years
- Qualification: B.Pharm / M.Pharm
- Work Type: On-site
- No. of Vacancies: 02
Job Description
Synergen Bio is seeking a Research Associate-I for its Clinical Quality Assurance department. The role focuses on ensuring GCP compliance, conducting audits, and maintaining quality standards across clinical bio studies. This position plays a vital role in supporting regulatory adherence and data integrity in clinical research operations.
Research Associate-I – Clinical Quality Assurance
- Department: Clinical Quality Assurance
- Role: Research Associate-I
- Experience: 3+ Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Strong knowledge of GCP, SOPs, and regulatory guidelines
- Experience in clinical trial audits and quality systems
- Excellent documentation and communication skills
- Ability to work independently and handle multiple tasks
- Attention to detail with problem-solving mindset
- Immediate availability preferred
Key Responsibilities
- Conduct in-process audits of clinical bio studies
- Perform retrospective audit of raw data and study reports
- Implement corrective actions on QA observations
- Update and report audit status to Head-QA
- Provide GCP and regulatory training to employees
- Prepare and review SOPs for system compliance
- Carry out system, facility, and vendor audits
- Manage deviation reports and trend analysis
- Handle document generation, reconciliation, and storage
- Verify calibration and validation records
Benefits/Perks
- Career growth in clinical research and QA domain
- Learning opportunities in global regulatory standards
- Exposure to advanced clinical quality systems
- Collaborative work culture focused on excellence
- Long-term stability in a growing CRO
How to Apply
Interested candidates should share their updated CV to careers@synergenbio.com. Mention the position “Research Associate-I – Clinical Quality Assurance” in the subject line. Immediate joiners will be given preference.
For more pharma jobs and clinical research opportunities across India, visit Pharma Recruiter.
Apply now to join a quality-driven clinical research team!
Why You Should Join
Synergen Bio offers a professional environment that values quality, innovation, and compliance. Employees benefit from continuous learning, recognition for contributions to clinical excellence, and long-term career growth. Join a team committed to maintaining the highest standards in clinical trials and help advance pharmaceutical research with integrity and precision.
FAQs
Q1: What is the experience required for this role?
A: Minimum 3+ years of relevant experience in Clinical Quality Assurance.
Q2: What qualifications are needed?
A: B.Pharm or M.Pharm graduates are eligible.
Q3: Is this a walk-in interview?
A: No. Applications are accepted via email only.
Q4: How many vacancies are available?
A: 02 vacancies for Research Associate-I.
