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Clinical Research Associate

2+ years
Not Disclosed
10 March 3, 2025
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm/Pharm D/BDS/MBBS 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

Clinical Research Associate

Location: Remote (Mumbai & Delhi)
Job ID: 2025-116816
Category: Clinical Monitoring
Company: ICON Strategic Solutions

About the Role:

Join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. This role offers a strong partnership-driven environment that values innovation and continuous improvement.

If you're looking for a workplace where you feel a sense of belonging, are empowered to reach your full potential, and can make a real impact in saving lives, this is the opportunity for you.

Key Responsibilities:

  • Perform all aspects of Clinical Research Associate (CRA) duties, including site selection, site initiation, routine monitoring visits, close-out visits, and database lock.
  • Work embedded within the client’s study team, with a dedicated ICON line manager for support.
  • Oversee study site management, ensuring high-quality data and maintaining low query levels.
  • Ensure compliance with Quality Assurance (QA) standards and generate quality reports.
  • Provide support and mentorship to other team members.

Qualifications:

  • Education: B.Pharm, M.Pharm, PharmD, BDS, or MBBS.
  • Experience: Minimum 2 years of onsite monitoring experience in Oncology (excluding training & induction).
  • Skills: Strong and clear communication skills.
  • Location: Mumbai & Delhi (Remote).