JSS Medical Research has announced a Clinical Research Coordinator job opening in New Delhi for candidates interested in clinical trials and research operations. The company is looking for professionals with 1–2 years of clinical research experience who understand Good Clinical Practice (GCP), study documentation, patient coordination, and regulatory requirements.

This JSS Medical Research Clinical Research Coordinator recruitment 2026 is particularly relevant for M.Pharm and M.Sc graduates seeking opportunities in the clinical research and CRO industry. Selected candidates will coordinate clinical studies, maintain essential documentation, support patient recruitment and study visits, and work closely with investigators and other study stakeholders.

JSS Medical Research Clinical Research Coordinator Job Overview

About the Clinical Research Coordinator Role

As a Clinical Research Coordinator at JSS Medical Research, you will support the day-to-day execution of clinical research studies according to the approved protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements.

The role involves coordination between investigators, study teams, research sites, patients or study participants, and other stakeholders. Candidates will also support clinical trial documentation, patient recruitment, screening, scheduling, follow-ups, data collection, monitoring activities, and query resolution.

Key Responsibilities

Selected candidates for the Clinical Research Coordinator job in New Delhi will be responsible for:

• Coordinating and supporting clinical research studies according to study protocols, SOPs, and applicable regulatory requirements.
• Maintaining study-related records, essential documents, and clinical trial documentation.
• Coordinating with investigators, clinical research teams, sites, and other stakeholders.
• Supporting patient and study-subject recruitment activities.
• Assisting with subject screening, scheduling, study visits, and follow-up activities.
• Ensuring timely and accurate collection and documentation of clinical study data.
• Supporting study visits and clinical trial monitoring activities.
• Assisting study teams with the resolution of data and documentation queries.
• Ensuring study activities comply with Good Clinical Practice (GCP) requirements.
• Following the approved clinical trial protocol and applicable regulatory requirements throughout study execution.

Qualification and Eligibility

According to the advertised job description, candidates should have one of the following postgraduate qualifications:

• M.Pharm in any specialization
• M.Sc in any specialization
• MS in a relevant science discipline

Candidates should also have approximately 1–2 years of relevant clinical research experience.

Applicants with practical knowledge of clinical trials, GCP guidelines, clinical study documentation, patient coordination, and regulatory compliance will be better aligned with the responsibilities of this position.

Skills Required

Candidates applying for the JSS Medical Research Clinical Research Coordinator vacancy should possess skills or knowledge in:

Clinical Research | Clinical Trials | Good Clinical Practice (GCP) | Clinical Study Coordination | Patient Recruitment | Patient Screening | Study Documentation | Regulatory Compliance | Clinical Data Collection | Study Visits | Query Resolution | Investigator Coordination | SOP Compliance

Strong organizational and communication abilities are also important because the Clinical Research Coordinator serves as an operational link between investigators, patients, study teams, and other stakeholders.

Salary

The advertised compensation for this Clinical Research Coordinator position is approximately:

₹2–3 lakh per annum

Actual compensation may depend on the candidate’s relevant experience, skills, existing compensation, and the company’s final employment terms.

Why Consider This Opportunity?

This position provides exposure to important aspects of clinical research operations, including:

• Clinical trial coordination
• Patient recruitment and screening
• Study visit management
• Essential clinical trial documentation
• Investigator and site coordination
• Clinical data collection
• GCP and regulatory compliance
• Monitoring support and query management

Professionals building a long-term career in clinical research, clinical operations, site management, or clinical trial coordination may find the experience relevant for future career progression.

Who Should Apply?

This opportunity may be suitable for candidates who:

• Have completed an M.Pharm, M.Sc, or MS qualification.
• Have around 1–2 years of clinical research experience.
• Understand GCP and basic clinical trial regulatory requirements.
• Have experience or knowledge of clinical trial documentation.
• Can coordinate effectively with investigators and study teams.
• Are comfortable supporting patient recruitment, screening, study visits, and follow-ups.
• Are interested in building their career in clinical research operations.

How to Apply

Application Link