Looking for a Clinical Research Associate (CRA) job in Ahmedabad or a Clinical Research Coordinator (CRC) role in India? Pellucid Lifesciences is hiring experienced professionals with 2โ5 years of clinical research experience to manage and oversee clinical trials. This opportunity is ideal for candidates with strong expertise in clinical trial management, GCP compliance, and site monitoring.
This CRA/CRC job in Ahmedabad offers hands-on exposure to clinical trial execution, regulatory compliance, and collaboration with CROs and clinical sitesโmaking it a strong career move in the clinical research domain.
Job Overview
- Role: Clinical Research Associate (CRA) / Clinical Research Coordinator (CRC)
- Company: Pellucid Lifesciences
- Location: Ahmedabad (Ashram Road)
- Experience: 2โ5 years
- Employment Type: Full-time
- Industry: Clinical Research / Pharma / Biotech
Key Responsibilities
As a Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC), you will:
- Manage and oversee clinical trials in coordination with CROs and study sites
- Ensure compliance with ICH-GCP guidelines, study protocols, and regulatory requirements
- Perform source data verification (SDV) to ensure data accuracy and integrity
- Monitor patient enrollment and adherence to inclusion/exclusion criteria
- Maintain and review essential clinical trial documents (ICFs, regulatory files)
- Act as a liaison between investigators, site staff, and CROs
- Identify and report adverse events (AEs) and protocol deviations
- Conduct site monitoring visits, audits, and inspections
- Support study planning, protocol development, and cross-functional coordination
- Maintain accurate clinical trial tracking and reporting systems
Qualifications & Requirements
To qualify for this CRA/CRC job in India, candidates should have:
- Bachelorโs or Masterโs degree in Pharmacy, Life Sciences, or related field
- 2โ5 years of clinical research experience
- Strong knowledge of GCP, ICH guidelines, and regulatory standards
- Experience in clinical trial monitoring and site coordination
- Excellent communication and project management skills
- Ability to work independently and within cross-functional teams
Salary & Benefits
- Estimated Salary: โน4,00,000 โ โน7,50,000 per annum (based on experience)
- Opportunity to work on end-to-end clinical trial management
- Exposure to regulatory compliance and global clinical research standards
- Career growth in CRA/CRC roles within pharma and biotech sectors
How to Apply
