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On-Site Research Assistant (Part Time) - Belagavi, Karnataka

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: Belagavi
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

This is a hospital-based clinical research support role where you assist in daily site operations of clinical trials.

👉 Translation: You are support staff at trial site, not decision-maker.


Key Responsibilities

1. Site Coordination

  • Act as point of contact for site communication

  • Coordinate study activities


2. Patient & Study Support

  • Assist in pre-screening participants

  • Support study-related tasks


3. Data Entry & Database Work

  • Enter clinical data into systems

  • Respond to system queries

  • Monitor study databases


4. Documentation & Compliance

  • Maintain documents as per **FDA / IRB guidelines

  • Ensure proper record keeping


5. Study Lifecycle Support

  • Assist in study closeout

  • Support ongoing trial activities


Required Skills

  • Basic clinical research understanding

  • Data entry & system handling

  • Communication & coordination

  • Organization & multitasking


Key Competencies

  • Clinical trial coordination

  • Documentation compliance

  • Site communication

  • Database handling


About the Company

ProPharma provides end-to-end services across regulatory, clinical research, pharmacovigilance, and quality domains.