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Ethics Committee Coordinator Cum Clinical Research Associate (Cra)

Edemera Global
Edemera Global
0-2 years
₹2,50,000 per annum
Hyderabad
10 March 20, 2026
Job Description
Job Type: Full Time Education: Pharm D 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

Ethics Committee Coordinator cum CRA | Fresher | Hyderabad | Edemera Global

Company: Edemera Global
Location: Hyderabad
Job Type: Full-Time
Experience: Fresher
Qualification: Pharm D (Mandatory)


Job Overview

This is an entry-level clinical research role combining Ethics Committee coordination and Clinical Research Associate (CRA) responsibilities. Ideal for fresh Pharm D graduates looking to enter the clinical trials industry.


Key Responsibilities

Ethics Committee Coordination

  • Prepare and submit documents to Ethics Committee (EC/IRB)

  • Maintain regulatory files and approvals

  • Ensure compliance with regulatory guidelines

Clinical Research Support

  • Assist in clinical trial activities and documentation

  • Coordinate with investigators and study teams

  • Support study monitoring and reporting


Required Skills

  • Basic knowledge of clinical research and GCP guidelines

  • Good communication and coordination skills

  • Attention to detail and documentation skills


Eligibility Criteria

  • Pharm D (Mandatory)

  • Fresher candidates only

  • Immediate joining availability


Compensation

  • Salary: ₹2.5 LPA


Application Process

  • Email your resume to: hr@edemeraglobal.com


Why This Role

  • Direct entry into clinical research field

  • Exposure to Ethics Committee + CRA work (dual experience)

  • Good starting point for CRA / Clinical Operations career