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Clinical Research Monitor Job at St Johns Bangalore | Salary: ₹50,000/Month

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St Johns

MBBS, BVSc, BDS, MPH, or a Postgraduate Degree

Rs.50,000/- per month

Bangalore

2 years

Verified Job

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Looking for a rewarding career in clinical research? Join the prestigious St Johns Medical College in Bangalore as a Clinical Research Monitor for the TIPS-3 PHRI Study. This exciting opportunity offers a chance to contribute to groundbreaking medical research while advancing your career in a dynamic, supportive environment. Read on to learn about the role, qualifications, benefits, and how to apply for this clinical research job in Bangalore.

Job Responsibilities

As a Clinical Research Monitor, you will play a critical role in ensuring the success of the TIPS-3 PHRI Study. Your key responsibilities include:

  • Monitoring Clinical Trials: Oversee study sites to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Data Collection and Reporting: Verify the accuracy of clinical data and prepare detailed reports for study sponsors.
  • Site Coordination: Collaborate with investigators and site staff to resolve issues and ensure smooth trial operations.
  • Travel: Conduct regular site visits across designated locations, ensuring adherence to study timelines and quality standards.
  • Documentation: Maintain accurate records of trial activities, including case report forms and regulatory documents.

This role demands precision, strong communication skills, and a commitment to advancing medical research in India.

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Qualifications and Skills

To excel as a Clinical Research Monitor at St Johns Medical College, candidates should meet the following criteria:

  • Educational Background:
    • MBBS, BVSc, BDS, MPH, or a Postgraduate Degree (including integrated PG degrees).
    • Alternatively, a Graduate or Postgraduate degree with a Diploma in Clinical Research.
  • Experience: Minimum of 2 years as a Site Clinical Research Associate (CRA).
  • Language Proficiency: Fluency in English, Kannada, Tamil, Telugu, and Hindi.
  • Skills:
    • Strong knowledge of clinical trial processes and GCP guidelines.
    • Excellent organizational and interpersonal skills.
    • Willingness to travel extensively for site visits.
  • Preferred: Candidates with prior experience in multi-site clinical trials and familiarity with the TIPS-3 PHRI Study protocols.

Benefits of Joining St Johns Medical College

Working at St Johns Medical College offers numerous advantages for clinical research professionals:

  • Competitive Salary: Earn a starting salary of ₹50,000 per month, with adjustments based on experience.
  • Career Growth: Access opportunities for professional development in clinical research and medical studies.
  • Impactful Work: Contribute to transformative research that improves healthcare outcomes globally.
  • Supportive Environment: Join a collaborative team at one of Bangalore’s leading medical institutions.
  • Work-Life Balance: Benefit from structured schedules and a focus on employee well-being.

This clinical research monitor position is ideal for professionals passionate about advancing medical science in Bangalore.

How to Apply

To apply for this Clinical Research Monitor role, follow these steps:

  1. Prepare a cover letter detailing your qualifications and interest in the TIPS-3 PHRI Study.
  2. Update your curriculum vitae (CV) with relevant experience and skills.
  3. Include contact details (names, email addresses, or phone numbers) for three professional references.
  4. Email your application to sangeetha.p@sjri.res.in, with a CC to hr@sjri.res.in.
  5. Submit your application by September 7, 2025.

Don’t miss this opportunity to join a leading clinical research team in Bangalore. Apply now to make a difference!

Frequently Asked Questions (FAQs)

Q: What is the TIPS-3 PHRI Study?
A: The TIPS-3 PHRI Study is a global clinical trial focused on evaluating interventions for cardiovascular health, conducted under the Population Health Research Institute (PHRI).

Q: Is travel mandatory for this role?
A: Yes, the Clinical Research Monitor position requires regular travel to study sites to ensure compliance and data accuracy.

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