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

2-5 years
Not Disclosed
10 June 12, 2025
Job Description
Job Type: Full 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

 

 

 


Clinical Research Associate at AstraZeneca India

Job Summary

AstraZeneca, a global leader in biopharmaceutical innovation, is hiring a Clinical Research Associate (CRA) in India. This full-time, on-site role focuses on delivering excellence in clinical study management and supporting the development of life-changing medicines. Ideal for candidates passionate about clinical development, regulatory compliance, and process improvement in a dynamic and collaborative environment.


Key Responsibilities

  • Execute processes for study delivery, including development of reports and tools.

  • Ensure consistent delivery of centrally managed study services from start-up to final reporting.

  • Act as the primary contact for document management until Clinical Study Report finalization.

  • Manage production and maintenance of study documents with template/version control.

  • Coordinate with Data Management teams to ensure timely document delivery.

  • Track study materials, equipment, and administrative tasks during audits and inspections.

  • Serve as a technical expert within Patient Safety, maintaining process knowledge.

  • Collaborate with compliance teams to enhance regulatory processes.

  • Identify opportunities for process improvement in clinical development methodology.


Required Skills & Qualifications

  • Essential:

    • Bachelor's degree in a relevant field.

    • Proven experience in study management within pharmaceutical or clinical settings.

    • Strong knowledge of clinical development regulations and best practices.

  • Desirable:

    • Advanced degree or professional certification.

    • Broad understanding of multiple study management aspects.

    • Familiarity with clinical documentation tools and global document libraries.


Perks & Benefits

  • Opportunity to work in a global biopharmaceutical company.

  • Access to lifelong learning and professional development programs.

  • Inclusive and diverse workplace culture.

  • Collaborative and supportive team environment.

  • Career growth within an innovative, patient-focused organization.


Company Description

AstraZeneca is a globally recognized biopharmaceutical company committed to discovering, developing, and commercializing prescription medicines for some of the world’s most serious diseases. With a strong presence in India for over 45 years, AstraZeneca continues to drive innovation and excellence in patient care, clinical development, and sustainability.


Work Mode

On-site (India)


Call to Action

Ready to make a meaningful impact in global healthcare? Apply now to join AstraZeneca’s dynamic clinical research team and contribute to pioneering advancements in medicine.