Designation | Scientist/Sr Scientist - Clinical |
Job Description | Support medical officers in the conduct of clinical trials Handle operational issues for clinical trials, including liaising with CROs and sites Ensure documentation in compliance with ICH-GCP for all trials Maintain and write additional SOPs , as required, for conduct of clinical research Prepare key trial related documents such as CRFs, ICF, and IB (where applicable) Be the primary channel of communication on study conduct with Investigators, CROs Trial management activities such as monitoring of sites, audit of CROs, training CRO personnel, monitoring of study participation Assist Trial managers in trial management Pre-trial activities such as interacting with vendors, processing RFQs, accrual planning, assist with conduct of DSMBs Prepare presentations, analyze trial related data including performance statistics for the trial as needed. Review site audit reports, CAPA and responsible for registration of trials with Trial registries. |
Desired Profile | MSc or MPharm with minimum 1-2 years of experience in clinical trial management. Must have sound knowledge of ICH-GCP and clinical trial process must possess excellent communication skills, and logical thinking hands on experience in managing trials a must knowledge of oncology trials a plus |
Experience | 1 - 4 Years |
Industry Type | Pharma/ Biotech/Clinical Research |
Role | Clinical Research Associate/Scientist |
Functional Area | Engineering Design, R&D |
Education | UG - Any Graduate - Any Specialization,Graduation Not Required PG - Any PG Course - Any Specialization,Post Graduation Not Required |
Location | Bengaluru/Bangalore |
Keywords | clinical trials ,ICH - GCP |
Contact | Arvind Padmanabhan Biocon Limited 20th KM Hosur Road Electronic City BANGALORE,Karnataka,India 560100 |
Telephone | 91-80-28082216 |
Website | http://www.biocon.com/ Apply Online |
Sunday, July 25, 2010
Scientist/Sr Scientist - Clinical - Biocon Bangalore
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