Clinical Research Associate

Terapia - a SUN PHARMA Company; Delhi; On-site; CAD 60,000 - 85,000; Full time

Job summary

A leading pharmaceutical company seeks a Clinical Research Associate to oversee clinical trials, including site monitoring and investigator training. The ideal candidate holds a Bachelor's or Master's degree in a health-related field and has 1-5 years of relevant experience. This role is essential for ensuring compliance and efficient data management in clinical research.

Qualifications

• Minimum qualifications: Bachelor's/Master's degree in health-related field.
• 1-5 years relevant experience in Clinical Research is required.

Responsibilities

• Perform site feasibility and negotiate study budget with investigators.
• Ensure timely site initiation, monitoring, close-out, and reporting.
• Train investigator and site personnel on study protocol and GCP principles.

Skills

Site feasibility

Investigator training

Data management

Budget negotiation

Inventory management

Education

Bachelor's or Master's degree in a health-related field

Post-graduate Diploma in Clinical Research

Job description

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Title: Clinical Research Associate

Date: Jun 6, 2025

Location: Delhi - Office

Company: Sun Pharma Laboratories Ltd

YOUR TASKS AND RESPONSIBILITIES:

• Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts
• Preparation and submission of study documents for EC permission for respective study across centers
• Oversee & document IP dispensing, inventory management & reconciliation
• Ensure timely site initiation, site monitoring, and site close-out activities are performed and respective reports are generated
• Investigator and site personnel training on the Study protocol, procedures, and GCP principles
• Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification and query resolution
• Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Suns PV policies
• Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
• Co-ordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
  
  

WHO YOU ARE:

• Minimum qualification requirement is to have a Bachelor's or Masters degree in a health[1]related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health and/or Post-graduate Diploma in Clinical Research
• Relevant experience of 1-5 years minimum in the field of Clinical Research
  
  

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