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Site Solutions Executive (Pri) - Delhi, India

0-4 years
4-8 LPA
Delhi, New Delhi, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Site Solutions Executive (Clinical Research Site Coordinator)

Company: Premier Research
Location: Delhi
Work Mode: Office-Based
Job Type: Full-Time


Experience Level

  • Bachelor's or Master's degree in:

    • Life Sciences

    • Clinical Research

    • Biotechnology

    • Biological Sciences

    • Nursing

    • Pharmacy

    • Medical/Dental Sciences

  • 0–4 years of Clinical Research experience

  • Freshers with relevant clinical research exposure may be considered

  • Entry to Junior-Level Position


Salary

Estimated market salary: ₹4–8 LPA CTC, with experienced Site Coordinators/Site Management professionals potentially earning ₹8–12 LPA.


Role Summary

The Site Solutions Executive supports the day-to-day management of clinical trials at investigator sites. The role works closely with Principal Investigators (PIs), study coordinators, sponsors, and CRO teams to ensure clinical trials are conducted in compliance with protocol requirements, ICH-GCP guidelines, regulatory requirements, and patient safety standards.


Key Responsibilities

Clinical Trial Coordination

  • Coordinate clinical trial activities at assigned sites.

  • Support investigators and study teams throughout the study lifecycle.

  • Ensure protocol compliance and adherence to regulatory requirements.

  • Assist in smooth execution of study procedures.


Site Management

  • Review site processes and identify operational gaps.

  • Support implementation of site process improvements.

  • Maintain site readiness for sponsor and regulatory inspections.

  • Ensure study documentation is complete and audit-ready.


Data Management

  • Perform accurate and timely data entry into:

    • CRFs (Case Report Forms)

    • eCRFs (Electronic Case Report Forms)

  • Coordinate with investigators to ensure data accuracy.

  • Support query resolution activities.


Documentation & TMF Management

  • Maintain Trial Master File (TMF) and essential documents.

  • Organize regulatory and study-related records.

  • Ensure documentation compliance with GCP standards.


Site Visit Support

  • Assist during:

    • Site Initiation Visits (SIV)

    • Monitoring Visits

    • Close-Out Visits

    • QA Audits

    • Sponsor Visits

    • Regulatory Inspections

  • Prepare required documentation and logistics.


Performance Tracking

  • Monitor and report site performance metrics.

  • Track recruitment and study progress.

  • Escalate operational challenges when required.


Required Qualifications

Education

  • BSc / MSc Life Sciences

  • B.Pharm / M.Pharm

  • BDS / MBBS

  • BSc Nursing / MSc Nursing

  • Biotechnology or Biological Sciences

  • Clinical Research qualifications

Professional Experience

  • 0–4 years of experience in:

    • Clinical Research

    • Clinical Trial Operations

    • Site Coordination

    • Clinical Data Management

    • Hospital Research Units


Key Skills

  • Clinical Trial Coordination

  • ICH-GCP

  • Investigator Site Management

  • eCRF/CRF Management

  • Trial Master File (TMF)

  • Clinical Documentation

  • Regulatory Compliance

  • Patient Coordination


Preferred Skills

  • Site Management Organization (SMO) Experience

  • CRO Experience

  • Clinical Trial Monitoring Exposure

  • Ethics Committee Coordination

  • Recruitment Tracking

  • Audit & Inspection Support


Language Requirements

  • Fluent English (Written & Spoken)

  • Hindi (Reading, Writing & Speaking)

  • Additional local language preferred


Soft Skills

  • Communication Skills

  • Attention to Detail

  • Organizational Skills

  • Problem Solving

  • Patient-Centric Mindset

  • Time Management

  • Team Collaboration


Ideal Candidate

A Clinical Research professional interested in site operations and clinical trial execution. This role is especially suitable for Life Sciences, Pharmacy, Nursing, and Clinical Research graduates looking to build a long-term career in Clinical Operations.