Discover clinical research jobs and QA jobs at Aizant. Advance your pharma careers in India with 2-4 years experience in drug development and compliance.
Contents
About the Company
Aizant Drug Research Solutions Pvt. Ltd., founded in 2008 and headquartered in Hyderabad, India, is a leading contract research organization (CRO) delivering integrated drug development solutions.
Specializing in CDMO, CMO, and CRO services, it excels in clinical research, bioanalytical testing, BA/BE studies, and formulation development for global pharmaceutical clients.
Committed to innovation and GxP regulatory compliance, Aizant fosters growth through advanced facilities and ethical practices, serving biotech and pharma industries worldwide.
Job Details
- Company Name: Aizant Drug Research Solutions Pvt. Ltd.
- Experience: 2 to 4 years
- Qualification: Any Graduate/Postgraduate for Archivist; B.Pharm/M.Pharm (PCI registration) for Pharmacist
- Location: Kompally, Hyderabad, Telangana
- Work Type: On-site
Job Description
Aizant is expanding its clinical QA and research teams in Hyderabad, seeking professionals to enhance document management and trial operations. These clinical research jobs emphasize GxP compliance and regulatory adherence in drug development. Join a leader in CRO services for impactful contributions to global health.
Jr. Archivist – Clinical QA
- Department: Clinical Quality Assurance
- Market: Drug Development
- Role: Manage and archive regulated documents per GxP standards
- Experience: 2 to 4 years
- Education/Qualification: Any Graduate/Postgraduate
Pharmacist – Clinical Research
- Department: Clinical Research
- Market: Trial Operations
- Role: Handle drug dispensing and accountability in trials
- Experience: 2 to 4 years
- Education/Qualification: B.Pharm/M.Pharm (PCI registration mandatory)
Skills/Qualifications
- Proficiency in GxP regulations and QA documentation standards
- Experience in archiving clinical trial documents and records
- Knowledge of clinical trial protocols and drug accountability
- PCI registration and hands-on pharmacy practice for research roles
- Strong organizational skills for managing regulated materials
- Familiarity with regulatory compliance in CRO environments
Key Responsibilities
- Organize and archive clinical documents per GxP guidelines
- Ensure timely retrieval and secure storage of QA records
- Dispense clinical trial drugs with accurate accountability
- Maintain documentation for trial compliance and audits
- Collaborate with teams on regulatory submissions
- Monitor inventory and report discrepancies promptly
Benefits/Perks
- Career growth in a trusted global CRO leader
- Continuous training in clinical research technologies
- Competitive salary with performance incentives
- Collaborative culture promoting innovation
- Exposure to international drug development projects
How to Apply
Email your updated CV and relevant documents to sonyjeevitha.degala@aizant.com, specifying the position. Immediate joiners preferred.
Verified Post
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Why You Should Join
Aizant Drug Research Solutions cultivates a culture of excellence and recognition, where your QA and pharmacy expertise accelerates innovative drug trials for worldwide impact.
With over 15 years of stability and global partnerships, enjoy secure long-term careers enriched by skill-building in compliant, forward-thinking labs that empower dynamic professionals to advance health outcomes.
FAQs
What qualifications are needed for the Jr. Archivist role?
Any Graduate/Postgraduate with 2-4 years in GxP document management.
Is PCI registration required for the Pharmacist position?
Yes, mandatory for B.Pharm/M.Pharm candidates in clinical research.
Where is the job location for these pharma jobs?
Kompally, Hyderabad—ideal for local talent in Telangana.
What growth opportunities does Aizant offer?
Advancement in CRO operations with training and global project involvement.