Job Description

Job Summary:

• Execute study and system-related activities following SOPs, GCP, GLP, and regulatory requirements.

Key Responsibilities:

• Conduct activities according to Apotex’s SOPs, regulatory guidelines, and safe work procedures.
• Input study data into required formats/databases for report preparation.
• Collect, record, and verify clinical study information.
• Perform requisition, receipt, and accountability of study materials.
• Ensure departmental audit readiness by maintaining good documentation practices and compliance.
• Organize files and clinical data for database entry.
• Assist in reconciling study data and coordinating with cross-functional teams.
• Handle clinical study materials, ensuring proper storage and issuance.
• Adhere to compliance programs, global quality policies, and safety/environmental standards.

Candidate Profile

Qualifications:

• B.Pharm, Pharm.D, or B.Sc in Life Sciences or related fields.

Skills and Abilities:

• Proficiency in MS Office.
• Effective communication skills.
• Flexible working hours.

Experience:

• 0-2 years in clinical research.

Additional Details

• Location: Bangalore, India
• Industry: Pharma/Healthcare/Clinical Research
• End Date to Apply: 30th December 2024

Application Link