TechObserver india Hiring Clinical Research Associate Noida

TechObserver india Hiring Clinical Research Associate
  • Full Time
  • Noida

Tech Observer India Job Vacancies

Tech Observer India, a leading Clinical Research Organization (CRO) with global expertise, is hiring for the role of Clinical Research Associate (CRA) in Noida. This is a full-time, permanent position designed for candidates with significant experience in onsite monitoring for Phase II, III, and IV clinical trials.

If you are passionate about clinical research and have a solid understanding of Good Clinical Practice (GCP) and Schedule Y, this opportunity could be your next career milestone.


Clinical Research Associate Recruitment Notification

Tech Observer India has been a trusted partner in the clinical research industry since 2005. With headquarters in New Jersey, USA, and a presence in over 20 countries, Tech Observer collaborates with top pharmaceutical companies to deliver innovative solutions and analytical support.

Job Details

  • Role: Clinical Research Associate
  • Location: Noida
  • Experience Required: 2+ years onsite monitoring experience in Phase II/III/IV studies
  • Employment Type: Full-time, Permanent
  • Industry: Clinical Research / Contract Research

Key Responsibilities

  • Conducting onsite monitoring visits, including Site Initiation Visits (SIVs), Monitoring Visits (MVs), and Close-Out Visits (CVs) for clinical studies.
  • Assisting the Project Manager in daily operations to ensure smooth project execution.
  • Supporting site feasibility, site selection, and clinical trial monitoring.
  • Ensuring compliance with GCP guidelines and regulatory standards.
  • Reviewing and verifying trial data to maintain accuracy and integrity.
TechObserver india Hiring Clinical Research Associate
TechObserver india Hiring Clinical Research Associate

Required Skills

  • Education: Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy).
  • Experience: Minimum of 2+ years in a CRA role with direct onsite monitoring experience.
  • Strong understanding of clinical trial protocols, GCP, and Schedule Y.
  • Proficiency in site feasibility, monitoring, and clinical operations.
  • Excellent communication and organizational skills.

Application Process

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Interested candidates are encouraged to apply via email. Send your updated resume to divya@tech-observer.com.

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Careers

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