Project Nurse II

St Johns Research Institute Sjri

2 - 7 years

2 - 5 Lacs

bengaluru karnataka india

Posted:19 hours ago| Platform: Foundit logo

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Skills Required

clinical assessment care coordination patient education data analysis regulatory compliance quality improvement

Work Mode

On-site

Job Type

Full Time

Job Description

Roles and Responsibilities:

Participant Management

Responsible for participant recruitment, informed consent process, and regular follow-ups as per study protocol.

Field Work & Sample Collection

Conduct field visits for community-based or site-based recruitment and collect biological samples such as swabs, blood, etc., adhering to study-specific protocols and safety procedures.

Monitoring & Coordination

Assist senior team members with coordination of clinical trial activities, including scheduling and conducting monitoring visits.

Training & Compliance

Undergo training on Good Clinical Practice (GCP) and study-specific procedures; train site personnel on GCP and protocol adherence.

Documentation & Support

Maintain accurate records of all participant interactions and sample collections; support the team with any other study-related tasks as needed.

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