Trainee Research Associate - Bioanalytical Department
Qualification: M.Pharm / B.Pharm/M.sc Life sciences
Experience: Freshers
To carry out the method development/validation/stutty sample analysis according to Good Laboratory Practices, in house SOP'S and working instructions
To comply with the GLP guidelines for managing the laboratory including safety, security and maintenance of the equipment
To monitor the techniques, analytical aboratory work involving vari various processing cal metho ods and standard operating procedures and complying with the GLP and approved protocols
Review of raw data and chromatographic data and continuously updating the status on ongoing studies to the investigator/manager.
Review of Method SOP's and bio-analytical reports of method validation and studies
To carry out the specific tasks like MD/MV, study sample analysis according to SOPs & working instructions of various equipment's and maintain related records
Retrieval of plasma, bulk spiking, processing of samples along with CC, QC's according to method SOP and written procedures
To comply with the GLP/applicable guidelines for managing the laboratory including the safety, security and maintenance of the equipment's
Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste
Preparation of bio-analytical reports, SOPs and Method SOPs.
Walk-In-Interview Date : 17th October 2024
Time : 9.30 AM - 12.30 PM
Venue: Axis Clinicals Limited.1-121/1. Survey Nos.66 (Part) & 67(Part. Gachibowli - Miyapur Rd. Serilingampalle (M), Telangana 500049
For More Information : +91-40-40408019
Email-Id : sampathkumar.p@axisclinicals.com
Candidates should carry his/her educational documents with them
AXIS Clinicals is an effective, metric-based clinical research organisation with a global footprint of operations. It is a privately held, well-established full-service CRO (Contract Research Organization) with its headquarters in Hyderabad, India (India, United States and Mexico).
AXIS Clinicals recognises the value of high-quality clinical research services, and our highly qualified staff works hard to offer them to our sponsors at significant cost savings. As a CRO with vertical integration, we provide specialised solutions to meet sponsor study requirements. We were founded in 2004 and provide trial management, monitoring, quality control, regulatory filings, data administration, and biostatistics, which enables us to put together a functional team that is best suited for each study. We have worked with a variety of clients, including large pharma and the developing biotechnology market.