Bharat Biotech International Limited is an Indian multinational biotechnology company headquartered in the city of Hyderabad, India engaged in the drug discovery, drug development, manufacture of vaccines, bio-therapeutics, pharmaceuticals and health care products.
UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY
In the global carbon cycle microorganisms have evolved a variety of methods for fixing carbon. Researchers from Bremen and Taiwan have investigated the methods that are utilized at extremely hot, acidic and sulfur-rich hydrothermal vents in shallow waters off the island of Kueishantao, Taiwan.
Antiseizure medication is usually prescribed for people with the condition. However, for one in three people with epilepsy around 20 million individuals worldwide, current antiseizure medications are ineffective. This means that people will continue to have seizures despite taking medication – a condition called ‘drug resistance.
As we age, blood stem cells, the essential source of new blood cells in the body, can accumulate genetic mutations. These mutations can give the cells a growth advantage, laying the foundation for developing serious health conditions. Now, scientists at The Jackson Laboratory (JAX) have not only discovered the mechanism that fuels their unchecked growth but have also found a way to stop it.
Professional having B.Pharm, BAMS, B-Tech, MPH. Preference will be given to professionals having experience in Digital Health. Foster partnerships with academia, industry, and international organization to accelerate digital health adoption.
Masters Degree in Chemistry, Pharmacy, Forensic Science specialization in Forensic Chemistry and Toxicology, Bio Chemistry from a recognized University. Assistant Director Chemistry and Toxicology, in Directorate of Forensic Services, Home Department
D.Pharm, Integrated Pharmacy Course for certificates issued by Government. vacant posts on a lump sum basis through the District Welfare Association on the basis of contract of the Siddha Medical Department.
To support the teaching needs of the M.Sc. in Clinical Research program with a specialization in Clinical Trials at THSTI.
Contribute ongoing and future clinical trials, epidemiological studies, and other health- related research projects by providing robust statistical expertise.
A Diploma in Pharmacy, Bachelor of Pharmacy. Must have registered with Pharmacy Council and must keep the registration alive by renewing it regularly every year.
BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.
TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts
Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines
As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.
Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software.
Strong analytical and problem- solving skills.
As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front. Broad understanding of the overall product and therapy along with deep technical expertise in one or more fields related to drugs and medical devices
The Clinical Data Management Associate is responsible for providing expert skills as part of the clinical data management team within the Data Management and Statistics Department to ensure that efficient and quality data management products are produced in accordance with customer requirements.
The Senior Specialist, Expert License Management prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.