ICBio Clinical Research – Walk-In Drive on 27th – 28th July 2024 for B.Pharm / M.Pharm / M.Sc Freshers & Experience

ICBio Clinical Research is a full-service Contract Research Organization (CRO), based in Bangalore, INDIA, providing comprehensive, quality & integrated and an end to end clinical research solutions; Clinical Trials (Phase I-IV), BA / BE studies (Bioequivalence studies), Clinical Endpoint studies, provide quality clinical research solutions in India & across the world. We believe in using science for the greater betterment of humanity. As a result, whether you’re a physician, a drug developer, a hospital, a medical researcher, or a patient, we work around the clock to give answers to all of your health issues. That includes everything from improving diagnostic testing to assisting with the launch of new pharmaceuticals to providing new insights through data, all of which draws on a wealth of scientific knowledge.

  • Qualification: B. Pharm / M. Pharm / M.Sc 
  • Experience : 02-08+years
  • Role: Research Associates / Research Scientists / Analyst/ Operators
  • Location: Bangalore

Time and Venue:

27th – 28th July 2024

Venue: ICBio Clinical Research Pvt. Ltd.
#2, ICBio Tower, Devi Circle, Chikkabettahalli, Vidyaranapura, Yelahanka Main Road, Bangalore-560097. INDIA
E-mail: [email protected]

Job description:

Role and Responsibility:
1. Perform method development, method validation and execute methods for the analysis of study samples within the committed timelines.
2. Sample processing, analysis of plasma, blood, and serum samples from BA/BE studies as per applicable regulatory requirements.
3. Review of inventory of chemicals/solvents/supplies in BA department.
4. Prepare buffer solution and other required solutions during MD, MV and study.
5. Perform literature survey and to develop and validate bio-analytical methods.
6. Document the raw data forms, methods notebooks and logbooks in daily basis.
Execute all the activities accordance with SOPs/regulatory guidelines
7. Analysis of individual sample repeats, ISR and compilation of validated excel for MD, MV and study
8. Follow the Good Laboratory Practice (GLP) principles and safety in the bioanalytical laboratory.
9. Assist Research Scientist/Group leader in method development, method validation and sample analysis.