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.
- Knowledge of clinical research principles, regulatory requirements, and ethics in clinical trials.
- Familiarity with regulatory guidelines such as ICH-GCP, FDA regulations, and local regulatory requirements.
- Strong attention to detail and organizational skills for document management and regulatory compliance.
- Excellent communication skills, both verbal and written, with the ability to collaborate effectively in a team environment.
- 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
