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: 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: 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: 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: 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: Gain hands-on experience in bioavailability and bioequivalence studies.
• Learning Opportunities: Work in a regulatory-compliant environment and enhance your skills in clinical research.
• Career Growth: 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.