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On-Site Research Assistant (Part Time) - Nagpur, Maharashtra

Propharma
Propharma
0-3 years
Not Disclosed
India
10 March 19, 2026
Job Description
Job Type: Part 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)

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


Job Overview

Same role, different city. No hidden upgrade here.

This is a clinical trial site support role where you assist with coordination, data entry, and documentation in hospital-based research.


Key Responsibilities

Site Coordination

  • Handle 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 per **FDA / IRB guidelines

  • Ensure proper documentation


Study Closure

  • Assist in study close-out activities


Required Skills

  • Basic clinical research knowledge

  • Data handling & documentation

  • Communication & coordination

  • Organization & multitasking