CLINICAL RESEARCH ASSOCIATE
Company: Sun Pharma Laboratories Ltd.
Business Unit: Clinical Research
Location: Mumbai (Sun House – Corporate Office)
Job Type: Full-Time
Date Posted: 23 June 2026
JOB OVERVIEW
Sun Pharma is seeking a Clinical Research Associate (CRA) to support the planning, execution, monitoring, and management of clinical trials. The role involves site management, investigator coordination, regulatory submissions, patient recruitment oversight, safety reporting, and ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.
KEY RESPONSIBILITIES
Perform site feasibility assessments and identify potential investigators.
Negotiate study budgets with investigators and research sites.
Finalize investigators and sites for clinical studies.
Execute Confidentiality Disclosure Agreements (CDA) and study-related contracts.
Prepare and submit study documents for Ethics Committee (EC) approvals across study centers.
Oversee Investigational Product (IP) dispensing, inventory management, and reconciliation.
Ensure timely site initiation, routine monitoring visits, and site close-out activities.
Generate and maintain monitoring reports and study documentation.
Train investigators and site personnel on study protocols, procedures, and GCP principles.
Monitor patient recruitment progress and enrollment targets.
Ensure accurate and timely data entry, source data verification (SDV), and query resolution.
Monitor protocol compliance and data quality at study sites.
Ensure timely reporting of:
Serious Adverse Events (SAEs)
Suspected Unexpected Serious Adverse Reactions (SUSARs)
Safety communications to investigators and study sites
Identify study risks and implement corrective and preventive actions (CAPA).
Coordinate with CROs and internal teams for:
Data Management
Statistical Analysis
Statistical Reports
Database Lock (DBL) activities
Maintain compliance with regulatory requirements and company policies throughout the study lifecycle.
EDUCATIONAL QUALIFICATIONS
Bachelor’s Degree in:
Life Sciences
Biology
Chemistry
Nursing
Pharmacy
Public Health
OR
Master’s Degree in a related health science field
OR
Post Graduate Diploma in Clinical Research (PGDCR)
EXPERIENCE
Required: 2–5 Years
Clinical Research experience
Clinical Trial Monitoring experience
Site Management experience
Clinical Operations exposure preferred
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Remote, India | Siliguri |Illinois :
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Bulgaria | Vedant |Denmark :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
Romania |Belgium :
Wavre |Tipperary :
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Brinny | Ringaskiddy |Carlow :
Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
Donegal |Meath :
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Dún Laoghaire |Galway :
Galway |County Dublin :
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China | Quarry Bay |Liaoning :
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Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
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Amsterdam |North Brabant :
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Haarlem |South Holland :
Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Sheffield |Oxfordshire :
Witney |Ontario :
Richmond Hill | Renfrew | Uxbridge | Mississauga | North York | Australia |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Peru | Argentina |Brazil :
Brazil | Sao paulo |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
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Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
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Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
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Japan | Saitama |Tokyo :
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