Post Name Clinical Research Associate Date August 17, 2023 Short Info. Patanjali Research Foundation is an equal opportunity employer and does not discriminate against any applicant because of race, colour, religion, gender, national origin, age and physical disability.
Patanjali Research Institute Recruitment 2023 Overview
| Company Name | Patanjali Research Institute |
| Post Name | Clinical Research Associate |
| Job Type | Full Time Job |
| Experience | 0 to 2 years |
| Function/Business Area | Retail |
| Location | Haridwar |
| Category | Marketing |
| Official Website | Patanjali Research Institute |
| Salary | Upto 2.5LPA + Incentives |
About Patanjali Research Institute Company
A Clinical Research Associate (CRA) is a professional who plays a critical role in the field of clinical research. Their primary responsibility is to ensure that clinical trials are conducted in accordance with applicable regulations, guidelines, and protocols.
Why You Should Join
- Protocol Compliance: Ensure that clinical trials are conducted according to the approved study protocols, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements.
- Site Selection and Initiation: Identify and evaluate potential investigational sites for participation in clinical trials. Conduct site initiation visits, train site staff on protocol requirements, and ensure all necessary documentation is in place.
- Monitoring: Perform routine monitoring visits to assigned sites to verify the integrity of clinical data and ensure compliance with study procedures. Collect, review, and verify source documentation and case report forms (CRFs) for accuracy and completeness.
- Data Management: Collaborate with data management personnel to ensure accurate and timely data collection, reporting, and resolution of data queries. Review data listings and tables to identify discrepancies or inconsistencies.
- Safety Reporting: Monitor and report adverse events (AEs) and serious adverse events (SAEs) to the sponsor, ethics committees, and regulatory authorities as required by regulations and protocols.
Education Requirement
- Bachelor’s degree in a scientific or healthcare-related field (or equivalent experience) such as MSc. Clinical Research M. Pharm, Pharm D medical and Paramedical degree.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements (e.g., FDA, ICH).
- Prior experience working as a Clinical Research Associate or in a related role is preferred.