This role will lead a team of researchers to support projects related activities pertaining to
in vivo
oncology for different modalities (small molecules, biologicals, etc.) entailing new model development; screening and interpretation of resul...
...Analyzes, reviews, and interprets safety data, both non-clinical and clinical.
Performs medical review of ICSRs, and other drug safety information from multiple sources, including clinical trials, spontaneous and...
Jubilant Drug Discovery and Development Services (JDDDS), is part of the Jubilant LifeSciences family of companies with R&D Centers in India, USA and business offices in Asia, Europe and North America. JDDDS has a global reach and provides comprehen...
...be prescribed from time to time.
Qualifications
Posr graduation in
Pharmaceutical Sciences or related field with extensive post-doctoral experience in developing and characterizing sterile injectable drug prod...
...management and delivers high-quality deliverables
They work with consulting senior management to develop opportunities of improvement and... ...studies, clinical trials, regulatory require...
This role will lead a team of researchers to support projects related activities pertaining to in vivo oncology for different modalities (small molecules, biologicals, etc.) entailing new model development; screening and interpretation of results, ge...
...Analyzes, reviews, and interprets safety data, both non-clinical and clinical.
Performs medical review of ICSRs, and other drug safety information from multiple sources,
including clinical trials, spontaneous ...
...Chemsys (Chemistry services) and Jubilant Clinsys (Clinical trial services). With over 1200 highly skilled and experienced scientific and medical personnel spread across Bangalore and Noida in India, Europe and the ...
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical develop...
...various conditions, in accordance with regulatory guidelines.
# Collaborate cross-functionally with formulation scientists, process chemists, and regulatory affairs professionals to support drug development progra...
