Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Research Associate (Cra)

Clinaarc
2-3 years
Not Disclosed
Bhubaneswar, Mumbai, Pune, India
3 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines

Clinical Research Associate (CRA)

Location: Mumbai, Pune, Bhubaneswar
Experience: 2–3 Years
Qualification: Life Sciences / Pharmacy Graduate

Job Description

Clinaarc is seeking experienced Clinical Research Associates to support clinical trial monitoring and site management activities.

Key Responsibilities

  • Monitor clinical trial sites and study conduct.

  • Ensure protocol adherence and GCP compliance.

  • Conduct site initiation, monitoring, and close-out visits.

  • Review study documentation and source data.

  • Coordinate with investigators and site staff.

  • Support overall clinical trial operations.

Requirements

  • 2–3 years of CRA experience.

  • Strong knowledge of ICH-GCP guidelines.

  • Excellent communication and site management skills.

  • Willingness to travel as required.

Apply

Email your CV to: hr@clinaarc.com
Subject Line: Clinical Research Associate – Preferred Location