It gives us immense pleasure to announce that Vegas Hospitals has shown interest in hiring talent from Clinilaunch Research Institute
Dear Student, Greetings!! It gives us immense pleasure to announce that Vegas Hospitals has shown interest in hiring talent from Clinilaunch Research Institute About: Vegas Hospitals Vagus Super Speciality Hospital is a technology based Multi-Super Speciality Hospital is centrally located in 18th Cross, Malleswaram, Bengaluru. Vagus Hospital is catring for head-to-toe health requirements of the human body and mind. Vagus Hospital is equipped with world standard equipment and imaging specialties to cover all specialty and super specialty facilities and services Website: https://www.practo.com/bangalore/hospital/vagus-superspeciality-hospital-malleswaram Job Type: Private Hiring For: Vegas Hospitals Job Role: CRC Internship (Clinical Research Coordinator) Industry: Hospitals and Health Care Job Priority: Normal Job Nature: Office Job Mode: Full Time Job Position: Intership (Based on interview you will Permanent) Job Location: Malleshwaram, Bengaluru, Karnataka Intership duration: 6 Months Salary: Stipend will be provided based on your interview performance Maximum 5k Experience Range : Fresher Interview Mode: Walk -In Interview date: 15.07.25 onwards Qualification: Life Science Graduates Date Published: 08-07-2025 Valid Through: 09-07-2025 (06.00 PM) Job Description: Trainees will receive hands-on training in clinical trial operations and will be closely mentored by experienced professionals in a real-time hospital setting. Eligibility Criteria: Strong interest in clinical research and willingness to learn. Good communication and interpersonal skills. Basic knowledge of clinical trial concepts is a plus. Responsibilities: Coordinate and manage clinical trial activities while ensuring adherence to study protocols and regulatory requirements Recruit, screen, and obtain informed consent from eligible study participants. Accurately collect, document, and manage clinical trial data. Maintain effective communication with investigators, sponsors, and study teams. Monitor participant safety and report adverse events in compliance with regulatory guidelines. Ensure compliance with Good Clinical Practice (GCP) and applicable ethical standards. Assist in training study staff and maintaining up-to-date regulatory and study-related documentation. Oversee trial logistics including management of supplies and investigational products. Application link: https://forms.gle/qoTVEMV5gqyTUwA47 For any queries contact Name: Mugesh Raj B and Priyanka C Contact No: 8951764077 & 8904527576