Dear Student, 
Greetings!!
It gives us immense pleasure to announce that Santhosh Hospital has shown interest in hiring talent from Clinilaunch Research Institute

About: Santhosh Hospita l

Welcome to Santhosh   Hospitals - Transforming Lives Through Compassionate Healthcare. At Santhosh Hospitals, we are driven by a singular commitment: to provide exceptional healthcare that goes beyond treatment to touch lives and transform communities. With a legacy rooted in compassion, innovation, and excellence, we stand as a beacon of healing, fostering a healthier. Our Vision: To be the forefront of transformative healthcare, delivering unparalleled medical solutions with a human touch. We envision a world where health is not just a state but a vibrant experience of well-beingWebsite: https://www.santoshhealthcare.com/

Job Type: Private

Hiring For: Santhosh Hospital

Job Role : CRC Internship (Clinical Research Coordinator)

Industry: Hospitals and Health Care

Job Priority: Normal

Job Nature: Office

Job Mode : Full Time

Job Position: Internship (based on performance will get Permanent)

Job Location: Infantry Road Bangalore, Karnataka

Internship 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/NoXXyC5MnhpMrxaz8 

For any queries contact 

Name: Mugesh Raj B and Priyanka C
Contact No: 8951764077 & 8904527576