Ph.D Biotechnology, Biochemistry, Bioinformatics or relevant branch of biological sciences with at least 1 research paper in Science Citation Indexed Journal.
Post Graduate Diploma in Clinical Trials or equivalent with at least 60% marks. At least one-year experience in clinical research. Experience in recruiting patients in clinical trials, familiarity with good documentation practices and good clinical practices.
All the full-time Ph.D. students admitted into the Ph.D. program will receive fellowship up to a maximum of five years. The fellowship could be from the Institute or Sponsored Projects. Ph.D. students may also have their own fellowship if qualified through UGC/CSIR NET.
Ability to conceptualize and drive large-scale marketing strategies with an execution-first approach. Experience in leading teams, collaborating with sales, and driving prescription demand at a national level.
Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA. Review of Analytical Method Validations, Method Transfers, Protocols & Reports. Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review.
Innovent Biologics, Inc , a world-class biopharmaceutical company that develops, manufactures and commercializes high quality medicines for the treatment of oncology, cardiovascular and metabolic, autoimmune, ophthalmology and other major diseases, announces that the first participant has been successfully dosed with IBI354
Diploma in Pharmacy D.Pharm or Bachelor of Pharmacy B.Pharm or Doctor of Pharmacy Pharm.D from a recognized University, Institution. Should be a registered Pharmacist under Pharmacy Act 1948.
Research experience in Drosophila genetics and epigenetics will be preferred. Masters degree in Natural or Pharmaceutical sciences and Three years of experience in Research and Development in industrial and academic institutions or Science and Technology organizations and scientific activities and services.
Project management for CoE-Antiviral and Antibacterial Drug Discovery and Development project and timely submission of progress reports to Director and nodal ministry. Proactively coordination of the project with various stakeholders and Principal Investigators of the project.
Doctoral Degree in Science, Engineering, Technology, Pharma from a recognized University or equivalent; Experience in Research & Development in Industrial & Academic Institutions or Science and Technology Organizations and Scientific activities and services
Experience of conducting and writing Systematic Reviews and Meta-analysis minimum two published systematic reviews as lead author. Knowledge about GRADE methodology. Experience in Statistics and Epidemiology
Hands-on experience in DNA sequence data analysis from FASTQ files, particularly on Human genomic or Metagenomic samples using standard data analysis pipeline. M.Sc / M.Tech in Life Science or experience in bioinformatic analysis of genomic/meta genomic data or Ph.D.in Life Science
M.Sc in Life Sciences, Chemistry from a recognized University or equivalent AND selected through a process described through anyone of the following National Eligibility Tests – CSIR-UGC NET including lectureship Assistant Professorship and GATE.
Review of various formulation and packing development, technology transfer documents like but not limited to Master Formula, Master Formula Card, Product Development Report, Dissolution Development report, Elemental Impurity Risk Assessment Report, Stability plan, QbD based Risk Assessment report, Failure Mode Effect Analysis, Process Validation Protocol
Use technical knowledge to perform in-depth review of API drug master file as per current US FDA expectations; identify deficiencies and formulate strategies to resolve them. Close coordination with Packaging material and Excipient vendors, placing orders, arranging technical documents to Analytical and Regulatory teams.
Bachelors degree in life sciences or business. Experience in consulting management in the life sciences, pharmaceutical/ biotech consulting industry or equivalent industry role
For the last six decades Central Government Health Scheme is providing comprehensive medical care to the Central Government employees and pensioners enrolled under the scheme. In fact CGHS caters to the healthcare needs of eligible beneficiaries covering all four pillars of democratic set up in India namely Legislature, Judiciary, Executive and Press.
Post graduate degree in Life Science. OR Graduate, Post Graduate Degree In professional course e.g., M.Sc. Pharmacology, M.Pharm, MBBS,BDS selected through a process described through any one of the following Scholars who are selected through National Eligibility Test- CSIR-USG, NET including lectureship (Assistant Professorship) and GATE, GPAT.
Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents. Writers and edits clinical regulatory documents, including submission summaries and other complex documents.
Ensures that direct reports have development and training plans, according to IDP process. Coaches the direct reports on a regular basis, and plans, organizes coaching with external providers if needed.