ICBio Clinical Research: CRO
Website:
icbiocro.com
Job details:
Company Description
ICBio Clinical Research. ICBio is a full-service CRO with 18+ years of experience, supporting global BA/BE studies, clinical trials (phases I–IV), and pharmacovigilance, and our studies are submitted across 56+ countries. We are approved by ANVISA Brazil, DCGI, MHRA, NPRA Malaysia, MOH Iraq, UAE MOH, GCC, Kazakhstan MOH, & Zambia, and many more. With 1000+ BA/BE studies and 500+ clinical trials completed, we ensure high-quality, timely, and cost-effective results. Served more than 80+ repeat clients from industries like pharmaceuticals, nutraceuticals, cosmetics, and medical devices for their regulatory requirements.
With a track record of 1000+ BA/BE studies and 500+ clinical trials submitted across 56 countries globally, our cutting-edge clinical facility includes 100 beds and features full access control, ensuring the highest levels of data integrity and patient care. We excel at delivering cost-effective, timely, end-to-end services tailored to the specific needs of your generic product. With our in-house NABL-accredited central lab with an integrated LIMS system, we ensure reliable clinical outputs backed by 100% data integrity and regulatory compliance.
Our Key Services:
• BA/BE Studies
• Clinical Trials Phase I–IV
• Pharmacovigilance & Biometric Services
Role Description
This is a full-time, on-site role for a bioanalytical scientist, located in Bengaluru. The bioanalytical scientist will be responsible for developing, validating, and implementing bioanalytical methods to support clinical studies. Daily tasks include conducting bioanalysis using advanced instrumentation, data analysis, preparing reports, and ensuring compliance with regulatory requirements. The selected candidate will collaborate with cross-functional teams to ensure the accuracy, reliability, and timeliness of data generated for clinical research studies.
Qualifications
- Proficiency in bioanalytical techniques such as LC-MS/MS, HPLC, and sample preparation methods
- Experience in developing and validating analytical methods according to regulatory guidelines
- Strong skills in data analysis, report preparation, and familiarity with statistical software
- Understanding of Good Laboratory Practices (GLP) and regulatory compliance frameworks
- Ability to troubleshoot and maintain bioanalytical instrumentation
- Effective communication and collaboration skills, with the ability to work in multidisciplinary teams
- Bachelor’s, Master’s, or Ph.D. degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field
- Prior experience in a bioanalytical environment or clinical research organization is a plus
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