Job Title

Job descriptionLocation:Mangalore/Rishikesh/Bhopal Multiple openings CTC: Rs 4-5 lakhsAbout the Role We are seeking an experiencedEngineer s to oversee hospital-based clinical trials for CanScan. The trial sites are Mangalore, Bhopal and Rishikesh. There are 3 openings, 1 in Mangalore, 1 in Bhopal and 1 in Rishikesh. The candidate should be willing to stay in Mangalore, Bhopal or Rishikesh till the completion of the trial with occasional travel to Pune for reporting. The role involveshands-on medical equipment operation, trouble shooting, servicing, inventory & logistics of consumables and maintenanceof the device for the successful trial completion. The person should ensure seamless trial execution, regulatory compliance, and high-quality reporting. The ideal candidate will collaborate closely with principal investigators (PIs), research assistants, and hospital staff to drive research success.Key Responsibilities Medical Equipment Handling :Oversee the setup, calibration, maintenance, troubleshooting of CanScan and consumables and accessories in hospital settings. Operation:Assist in monitoring CanScan’ssensor performance, calibration, and patient interactionduring trials. Clinical Trial Monitoring:Ensure protocol compliance, data accuracy, and efficient trial execution, identifying and mitigating potential risks. Report Writing & Documentation:Draftdetailed trial reports , capturing equipment performance, patient responses, and key clinical insights. Stakeholder Coordination:Engage withPIs, research assistants, and hospital administratorsto ensure alignment on trial procedures and findings. Regulatory & Compliance Management:Ensure adherence toGCP standards, hospital ethics approvals, and device-related regulatory frameworks . Overall Trial Management:Maintain documentation, oversee equipment logistics, and support trial teams in day-to-day operations. Qualifications & Requirements Degree in Biomedical/Electronics/Mechanical Engineering . Familiarity withmedical device handling and operationrequired. Prior involvement inmedical equipment validation . Excellentcommunication and organizational skillsto collaborate with medical and research teams.