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Fresher - Us Healthcare Operations - Benefit Analyst Junior - Jr178504

Carelon Global Solutions
Carelon Global Solutions
0-3 years
Not Disclosed
Gurugram, India
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

On-Site Research Assistant (Part-Time) – Kanpur, Uttar Pradesh

Company: ProPharma
Location: Kanpur
Job Type: Part-Time (24 hours/week)
Contract Duration: 1 Year (extendable)
Experience: Entry-level / 0–3 Years
Qualification: Bachelor’s Degree or equivalent


Job Overview

This is a hospital-based clinical research support role focused on site coordination, data entry, and documentation for ongoing clinical trials.


Key Responsibilities

Site Coordination

  • Manage communication between site and study teams

  • Coordinate daily clinical trial activities

Patient & Study Support

  • Assist in pre-screening participants

  • Support study execution

Data Entry & Monitoring

  • Enter and manage clinical data

  • Respond to system queries

  • Track study databases

Compliance & Documentation

  • Maintain records as per FDA / IRB guidelines

  • Ensure proper documentation and regulatory compliance

Study Closure

  • Assist in study close-out activities


Required Skills

  • Basic clinical research knowledge

  • Data handling and documentation

  • Communication and coordination skills

  • Organizational and multitasking ability