ICBio Clinical Research Walk-in Drive for Bioanalytical Department

ICBio Clinical Research Pvt. Limited, a renowned independent full-service Contract Research Organization (CRO), is excited to announce a walk-in drive for its Bioanalytical Department. This is an excellent opportunity for skilled professionals and fresh graduates to join a leading organization in the biosciences sector.

About ICBio Clinical Research

ICBio Clinical Research is a premier CRO specializing in Bioavailability/Bioequivalence (BA/BE) Studies, Clinical Trials Phase I-IV, pharmacovigilance, and clinical safety services. Committed to excellence in biosciences, ICBio partners with pharmaceutical and biopharmaceutical companies to deliver high-quality research and development services.

Walk-in Drive Details

Event: ICBio Clinical Research Walk-in Drive for Bioanalytical Department
Dates: 24th July 2024 to 28th July 2024
Time: 10:00 AM to 4:00 PM
Venue: ICBio Clinical Research Pvt. Ltd., #2, ICBio Tower, Devi Circle, Chikkabettahalli, Vidyaranapura, Yelahanka Main Road, Bangalore-560097, INDIA
Contact: hr@icbiocro.com

Positions Available

ICBio is looking for talented individuals to fill the following positions in the Bioanalytical Department:

• Research Associates
• Research Scientists
• Analysts
• Operators – LCMS

Qualifications and Experience

• Educational Qualification: M Pharmacy, B Pharmacy, MSc in Chemistry, Life Sciences
• Experience: 2-8 years in BA/BE Studies. Freshers are also encouraged to attend.

Job Responsibilities

Research Associates / Research Scientists / Analysts / Operators – LCMS

1. Method Development and Validation: Perform method development, validation, and execute methods for the analysis of study samples within committed timelines.
2. Sample Processing: Analyze plasma, blood, and serum samples from BA/BE studies as per applicable regulatory requirements.
3. Inventory Management: Review and manage the inventory of chemicals, solvents, and supplies in the Bioanalytical department.
4. Solution Preparation: Prepare buffer solutions and other required solutions during method development, validation, and study phases.
5. Literature Survey: Conduct literature surveys to develop and validate bioanalytical methods.
6. Documentation: Maintain accurate documentation of raw data forms, methods notebooks, and logbooks on a daily basis.
7. Sample Analysis: Perform analysis of individual sample repeats, Incurred Sample Reanalysis (ISR), and compile validated data for method development, validation, and study.
8. Good Laboratory Practice (GLP): Adhere to GLP principles and safety protocols in the bioanalytical laboratory.
9. Support Activities: Assist Research Scientists and Group Leaders in method development, validation, and sample analysis.