Looking for Clinical Research Associate jobs in Ahmedabad? Veeda CR has announced new openings for experienced Clinical Research Associates (CRA) in Ahmedabad. Candidates with 2-5 years of experience in clinical research site monitoring, ICH-GCP compliance, and regulatory documentation can apply for this opportunity.

This Clinical Research Associate job offers excellent exposure in clinical trial monitoring, site management, regulatory compliance, and sponsor coordination. Professionals seeking CRA jobs in India, clinical research jobs in Ahmedabad, or pharma CRO careers should not miss this opportunity.

About Veeda CR

Veeda Clinical Research Official Website

Veeda CR is a leading Contract Research Organization (CRO) providing clinical research, bioavailability, bioequivalence, and laboratory services to pharmaceutical and biotechnology companies globally.

Job Details

Key Responsibilities

Off-Site Monitoring Activities

• Conduct off-site visits during different phases of clinical studies.
• Perform Initial Site Visits (SIV) to train and guide site personnel.
• Ensure study sites are prepared as per protocol requirements.
• Conduct routine monitoring visits according to study guidelines.

Clinical Trial Documentation

• Prepare and review:
  • Pre-Study Qualification Reports
  • Site Initiation Visit Reports
  • Site Monitoring Visit Reports
  • Site Closeout Visit Reports
• Coordinate feasibility assessment questionnaires with clinical sites.
• Collect and maintain essential regulatory documents and calibration reports.
• Share study logs, recruitment trackers, and source data templates with sites.

Regulatory Compliance & Audits

• Review study documents as per SOPs, protocol requirements, and regulatory guidelines.
• Train site teams on:
  • ICH-GCP
  • Regulatory updates
  • Root Cause Analysis
  • Clinical trial compliance
• Respond to sponsor, QA/QC, and regulatory audit queries.
• Maintain audit readiness throughout the clinical trial lifecycle.

Eligibility Criteria

Candidates applying for this Clinical Research Associate role should possess:

• Bachelor’s or Master’s degree in:
  • Pharmacy
  • Life Sciences
  • Clinical Research
  • Biotechnology
• 2-5 years of experience in clinical trial monitoring.
• Strong understanding of:
  • ICH-GCP guidelines
  • Regulatory compliance
  • Site monitoring processes
  • Clinical trial documentation

Preferred Skills

• Clinical site monitoring
• Clinical trial management
• Regulatory documentation
• Audit handling
• Communication and coordination
• Site feasibility assessment
• Monitoring visit reporting
• Sponsor communication

Why Join Veeda CR?

• Opportunity to work with a reputed CRO in India.
• Exposure to global clinical trials and regulatory standards.
• Career growth in clinical research and trial management.
• Competitive salary package and professional learning environment.

How to Apply

Application Link