Clinical Research Monitor

Why This Role Matters
Clinical trials are essential for evaluating the safety, efficacy, and quality of new medicines before they reach patients. Drug-based clinical trials require strict monitoring, accurate documentation, and compliance with international regulatory guidelines to ensure reliable research outcomes. Monitoring clinical trial sites helps maintain data integrity, participant safety, and regulatory compliance throughout the study lifecycle.
The Clinical Research Monitor plays a critical role in supervising clinical trial activities at research sites. This role ensures that clinical trials are conducted according to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. By coordinating with investigators, research staff, and sponsors, the monitor ensures that clinical trial processes—from site feasibility to study closeout are performed correctly.
At St. John’s Research Institute (SJRI), Bengaluru, the Clinical Research Monitor position supports the TIPS‑3 PHRI Study, a drug-based clinical trial focused on advancing medical research and improving patient outcomes. Professionals in this role contribute significantly to maintaining the quality, safety, and scientific validity of the clinical trial.

Job Description
The Clinical Research Monitor will support ongoing clinical trials by coordinating site activities, assisting senior research staff, and monitoring study progress across clinical trial sites. The role includes conducting monitoring visits, providing training to site staff on GCP and study protocols, and ensuring that all trial activities follow regulatory guidelines.
The selected candidate will be involved in multiple phases of the clinical trial lifecycle, including site feasibility assessment, initiation visits, participant recruitment monitoring, follow-up phases, and study closeout activities. The role also requires handling audit readiness and supporting inspection processes to ensure compliance with international clinical research standards.

Key Features of the Role

• Job Title: Clinical Research Monitor (CRM) / Clinical Trial Monitor
• Project Type: Drug-Based Clinical Trial
• Research Organization: St. John’s Research Institute
• Study: TIPS‑3 PHRI Study
• Number of Vacancies: 1
• Job Location: Bangalore, India
• Work Nature: Clinical trial monitoring and site coordination
• Travel Requirement: Willingness to travel to clinical trial sites

Responsibilities

• Assisting senior researchers in coordinating and monitoring clinical trial activities.
• Undergoing training on clinical trial monitoring processes and regulatory requirements.
• Scheduling monitoring visits to ensure compliance with study protocols.
• Conducting monitoring visits at clinical trial sites to assess study progress.
• Providing training to site staff on Good Clinical Practice (GCP) guidelines and study procedures.
• Supporting documentation and data verification to maintain study accuracy.
• Ensuring clinical trial activities comply with regulatory and ethical standards.
• Coordinating with investigators and clinical staff during the recruitment phase of the study.
• Monitoring follow-up activities and participant progress throughout the trial.
• Supporting study closeout activities and documentation review.

Specific Clinical Trial Activities

• Site Feasibility Assessment
• Site Initiation Visits
• Participant Recruitment Phase Monitoring
• Follow-Up Phase Coordination
• Study Closeout Phase Activities
• For-Cause Monitoring Visits
• Audit and Regulatory Inspection Support

Required Qualifications

Educational Requirements

• MBBS (Bachelor of Medicine and Bachelor of Surgery)
• BVSc (Bachelor of Veterinary Science)
• BDS (Bachelor of Dental Surgery)
• MPHW with Postgraduate Degree
• Graduate or Postgraduate degree with a Diploma in Clinical Research
• Integrated postgraduate degrees in relevant healthcare or life sciences disciplines

Experience and Skills

• Minimum 2 years of experience working as a Site Clinical Research Associate (CRA) or similar clinical research role.
• Understanding of clinical trial monitoring and regulatory compliance.
• Knowledge of Good Clinical Practice (GCP) guidelines and clinical trial processes.
• Ability to coordinate clinical trial site activities effectively.
• Strong analytical and documentation skills.
• Willingness to travel for site monitoring visits.
• Ability to work collaboratively with clinical investigators and research staff.

Language Requirements

Candidates should have proficiency in multiple languages, including:
• English, Kannada, Hindi, Tamil, Telugu, Other relevant local languages

Salary Insights
The salary for the Clinical Research Monitor position is competitive and depends on the candidate’s experience and interview performance.
Estimated Salary: • ₹50,000 per month

Additional professional benefits may include:
• Hands-on experience in drug-based clinical trials
• Exposure to clinical trial monitoring and site management
• Opportunities to work with experienced clinical research professionals
• Career growth opportunities within clinical research organizations

Company Overview
St. John’s Research Institute (SJRI) is a leading biomedical research institution based in Bangalore, India. The institute conducts research in public health, clinical medicine, nutrition, infectious diseases, and chronic disease prevention.
SJRI collaborates with national and international research organizations to conduct high-quality clinical trials and health studies. The institute is recognized for its contributions to improving healthcare outcomes through evidence-based research and scientific innovation. Through studies such as the TIPS‑3 PHRI Study, SJRI supports the advancement of clinical research and contributes to global healthcare improvements.

FAQs

1. What does a Clinical Research Monitor do?
A Clinical Research Monitor supervises clinical trial sites to ensure studies follow protocols, regulatory guidelines, and Good Clinical Practice standards.

2. What experience is required for this role?
Candidates typically need at least two years of experience as a Site Clinical Research Associate (CRA) or in clinical trial monitoring roles.

3. Is travel required for this job?
Yes, clinical research monitors usually travel to different trial sites to conduct monitoring visits.

4. What skills are important for a Clinical Research Monitor?
Important skills include clinical trial knowledge, GCP compliance, communication skills, documentation accuracy, and problem-solving ability.

5. What career growth opportunities exist after this role?
Professionals can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Clinical Operations Manager.

Application Tips

• Highlight experience in clinical trial monitoring or site coordination.
• Demonstrate knowledge of Good Clinical Practice (GCP) and clinical trial processes.
• Mention any experience with site visits, monitoring reports, or audit preparation.
• Emphasize communication skills and the ability to coordinate with multiple research teams.
• Include certifications or diplomas related to clinical research if applicable.