Male Freshers - bioavailability & bioequivalence Studies

NOTE:

• Only Male & Candidates from Telangana Preferred.
• Kindly Understand the JD It's not for the Clinical Trails Department
• 2-Years Bond & Need to Submit your Original Mark list with us during the Bond Period.

Location: Aizant Drug Research Solutions Pvt Ltd, Dulapally (Unit-I) / Ameerpet (Unit-II)

1. Study Custodian
Requirements: B.Pharm or B.Sc
Key Responsibilities: Oversee study-related documentation and ensure compliance with regulatory standards.

2. Registration or Screening Officer

Requirements: B.Pharm or B.Sc

Key Responsibilities: Ensuring that study participants meet the necessary eligibility criteria before enrollment. Maintain detailed screening records for regulatory audits and study reports.

3. Clinical Quality Assurance

Requirements: M.Pharm

Key Responsibilities: Ensuring that all study activities comply with regulatory guidelines, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Documentation Practice (GDP). The QA team is responsible for preventing errors, ensuring compliance, and maintaining data integrity throughout the study lifecycle.

4. Quality Control

Requirements: M.Pharm

Key Responsibilities: Ensuring that the study processes, data, and results comply with regulatory requirements, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.

Interested can share resume to aishwaryarani.k@aizant.com