Aizant is a leading player in the pharmaceutical research and development sector, specializing in bioavailability and bioequivalence studies. With a strong reputation for adhering to regulatory standards and delivering high-quality research, Aizant offers a collaborative work environment and opportunities for professional growth.
Job Roles and Responsibilities
1. Study Custodian
- Requirements:Â B.Pharm or B.Sc
- Key Responsibilities:
- Oversee study-related documentation.
- Ensure compliance with regulatory standards and SOPs.
- Maintain accurate records for audits and reports.
2. Registration or Screening Officer
- Requirements:Â B.Pharm or B.Sc
- Key Responsibilities:
- Screen study participants to ensure eligibility.
- Maintain detailed screening records for regulatory audits.
- Coordinate with the research team for smooth study execution.
3. Clinical Quality Assurance
- Requirements:Â M.Pharm
- Key Responsibilities:
- Ensure compliance with GCP, GLP, and GDP guidelines.
- Monitor study activities to prevent errors and maintain data integrity.
- Conduct internal audits and prepare reports for regulatory submissions.
4. Quality Control
- Requirements:Â M.Pharm
- Key Responsibilities:
- Ensure study processes and results comply with regulatory requirements.
- Follow SOPs and GCP guidelines for quality assurance.
- Review and validate study data for accuracy and reliability.
Why Join Aizant?
- Industry Exposure:Â Gain hands-on experience in bioavailability and bioequivalence studies.
- Learning Opportunities:Â Work in a regulatory-compliant environment and enhance your skills in clinical research.
- Career Growth:Â Be part of a reputed organization with a focus on innovation and excellence.
How to Apply
Interested candidates can share their resumes with aishwaryarani.k@aizant.com. Make sure to mention the job role you are applying for in the subject line.
Advertisement