As a Scientist, Clinical Trial Safety, you will play a pivotal role in reviewing large amounts of clinical data to ensure patient data is complete and medically accurate. support the team during study start-up activities, review patient-level clinical/safety data on an ongoing basis, schedule and facilitate different types of meetings, and create visualizations from applicable tools.
Awareness, understands, and follows all relevant policies relating to this job including business, compliance, regulatory, quality, environmental, and safety expectations. Makes sound technical decisions, and appropriately communicates these decisions to other scientists and management.
Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit.
Candidates having M.Sc., M. Tech, M.Pharm., M.V.Sc. or equivalent qualification in Life Sciences or allied subjects Biochemistry, Biotechnology, Virology, Bioinformatics, Computational Biology, Microbiology, etc
Ph.D. degree in Microbiology, Biochemistry, Biotechnology subject from a recognized University with 5 years R&D,Teaching experience in the relevant subject after Ph.D
MSc, M.Tech, M.Pharm. in relevant stream of Biological Sciences with 3-5 years of relevant experience in Analytical R&D, QC department of Biopharmaceutical industry.
Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from recognized University or equivalent. Whole Genome Sequencing of MTB Clinical Strains for Determining Drug Resistance and Strain lineage