Clinical Research Associate Jobs at Cadila Pharmaceuticals | Apply Now
Are you looking for an exciting opportunity to build your career in clinical research? Cadila Pharmaceuticals Limited is hiring a Clinical Research Associate – Study Personnel (Toxicology & Efficacy) in Dholka, Gujarat. This role offers hands-on experience in animal studies, pharma-efficacy testing, toxicity studies, and compliance with GLP principles while working with one of India’s leading pharmaceutical companies.
About the Company:
Cadila Pharmaceuticals Limited is one of India’s largest privately held pharmaceutical companies, headquartered in Ahmedabad, Gujarat. With over six decades of innovation, the company is committed to providing affordable, high-quality medicines and has a strong presence in more than 100 countries. Cadila’s R&D centers are dedicated to driving advancements in healthcare, covering therapeutic areas such as oncology, cardiology, gastroenterology, and infectious diseases.
Job Details
Job Role: Clinical Research Associate
Location: Dholka, Gujarat
Job Responsibilities:
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Request and manage the required number of study animals.
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Observe study animals for clinical signs, functional observation battery, and mortality.
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Handle receipt, storage, and preparation of chemicals, reagents, and solutions.
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Prepare and administer dosing via different routes.
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Record animal weight, feed consumption, body temperature, and dermal observations.
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Perform randomization of study animals.
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Conduct pharma-efficacy studies, including batch release tests such as Pyrogen test, Abnormal toxicity test, Potency assays, and Nodule test.
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Collect, separate, and store blood samples.
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Compile and prepare study reports.
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Conduct studies, ensure accurate data collection, compilation, and verification.
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Collect samples/specimens and prepare verified reports.
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Participate in genotoxicity studies and standardization of new toxicity studies.
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Enter raw data into computer applications for analysis.
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Cooperate during internal, RQA, and sponsor audits of study plans, data, and reports.
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Ensure proper labeling of containers, test items, and samples.
Documentation:
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Document deviations from SOP or study plans and report to SD.
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Record raw data promptly, accurately, and in compliance with GLP principles.
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Maintain internal records as per in-house SOPs and GLP guidelines.
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Update and maintain training records.
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Ensure availability of monitoring certificates (feed, water, bedding, health).
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Request and maintain controlled/uncontrolled documents.
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Prepare and revise SOPs as required.
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Archive documents as per in-house SOPs.
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Verify calculations, compile results, and ensure proper data analysis.
Instrument Handling and Maintenance:
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Operate instruments according to SOPs and ensure calibration/maintenance.
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Perform calibration and maintenance of instruments as per in-house SOPs.
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