Responsibilities:

• Reporting and registration of volunteers.
• Obtaining ICF for registration of volunteers into the volunteer databank.
• Assisting in obtaining ICF for screening of volunteers.
• Measuring height and weight of volunteers and calculating BMI.
• Registering volunteers into the volunteer databank.
• Updating volunteer personal information in the database.
• Assisting in obtaining study ICF.
• Administering IPs by oral route.
• Performing custodian activities.
• Weighing and distributing meals.

1. Knowledge of clinical research principles, regulatory requirements, and ethics in clinical trials.
2. Familiarity with regulatory guidelines such as ICH-GCP, FDA regulations, and local regulatory requirements.
3. Strong attention to detail and organizational skills for document management and regulatory compliance.
4. Excellent communication skills, both verbal and written, with the ability to collaborate effectively in a team environment.
5. Proficiency in MS Office applications (Word, Excel, PowerPoint) for document preparation and data management.

Interested candidates, please share your resume at: aishwaryarani.k@aizant.com