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    • 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…
    • View all Sun Pharma Laboratories Ltd jobs - Delhi, Delhi jobs - Clinical Research Associate jobs in Delhi, Delhi
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    • Pharmacy or Life Science graduate.
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    • Full Time | 2.5 - 4.5 Lacs PA.
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  • Qualification: Any Graduate Type: Full Time Experience Required: -1-2 Years Location: Ayushman Hospital, Dwarka Sec – 10, New Delhi – 110075 Salary: Best as…

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Job Post Details

Clinical Research Associate - Delhi - job post

Sun Pharma Laboratories Ltd
4.3 out of 5 stars
Delhi, Delhi
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Location

Delhi, Delhi

Full job description

Title: Clinical Research Associate - Delhi

Date: Aug 4, 2026
Location: Delhi - Office
Company: Sun Pharma Laboratories Ltd
Job Title:

Clinical Research Associate

Business Unit:

Medical Affairs & Clinical Research

Location:

Delhi

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

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


Job Requirements

Educational Qualification

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

Experience

Relevant experience of 1-5 years minimum in the field of Clinical Research

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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