Clinical Research Monitor-TIPS-3 PHRI Study St Johns Research Institute Sjri

2.0 - 7.0 years

2 - 5 Lacs

bengaluru, karnataka, india

On-site

Roles and Responsibilities: Site Coordination Assist senior team members in the coordination of ongoing clinical trials at assigned sites. Training & Development Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP). Monitoring Activities Schedule and conduct monitoring visits to clinical trial sites in accordance with the study protocol and regulatory requirements. Site Support Provide training to site personnel on GCP guidelines and specific study-related activities to ensure compliance. Documentation & Reporting Ensure accurate and timely documentation of monitoring visits and maintain detailed records in line with trial protocols.

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Engineer-EHS Mold Masters

4.0 - 10.0 years

2 - 6 Lacs

noida, uttar pradesh, india

On-site

The Engineer-EHS shall be responsible for supporting the overall development, implementation, and continuous improvement of EHS programs to ensure compliance with local country regulations. The role involves data analysis, reporting, auditing, and site support to help mitigate risk and promote a safe and sustainable workplace. Work You ll Do: Collect, analyze, track and report EHS data including incidents, safety observations, near misses, and other metrics as required. Assist in the development and implementation of EHS programs of Hillenbrand programs, policies, and procedures. Support site incident investigations including root cause analysis and corrective action tracking. Conduct or coo...

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