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5.0 - 8.0 years
12 - 22 Lacs
bengaluru
Hybrid
Job Description Job Responsibilities: Works under general direction. Independently determines and develops approach to solutions. Contributes to a project of considerable significance or leads smaller scope projects. Supports material/design/packaging/process changes to the product line through design control process, with well documented research/analyses. Demonstrates accountability for successful and timely completion of designated tasks. Develops technical solutions to complex problems using sound engineering principles, utilizing experimental, computational, and analytical methods. Designs and develops in vivo and in vitro models to evaluate product/packaging features and improvements. ...
Posted 13 hours ago
0.0 - 4.0 years
0 - 0 Lacs
maharashtra
On-site
Role Overview: You will be a Post-Doctoral Fellow at The Kirby Institute, located in Kensington, NSW, working on laboratory-based research projects focused on detection techniques for neglected tropical diseases (NTDs) and other infectious diseases. Your role will involve contributing to studies assessing NTD burden in endemic countries, evaluating disease control strategies, participating in epidemiological studies, and collecting samples for laboratory analysis. Reporting to senior academic staff, you will perform key laboratory tasks, support data management, conduct statistical analysis, and disseminate findings. Depending on the level (A or B), your responsibilities will vary, including...
Posted 1 week ago
0.0 - 4.0 years
0 Lacs
surat, gujarat
On-site
A Clinical Research Coordinator is responsible for overseeing the trouble-free running of clinical trials, collecting data obtained from research, coding, and analyzing it. They manage budgets set aside for research and communicate with participants regarding study objectives. Administering questionnaires and monitoring participants to ensure they adhere to the study's rules is also part of their duties. The Coordinator liaises with laboratories regarding research findings and monitors the study to ensure it complies with protocols, is ethically-conducted, and follows regulatory standards. They are responsible for maintaining research records of study activity, including case report forms, d...
Posted 2 months ago
0.0 - 4.0 years
0 Lacs
roorkee, uttarakhand
On-site
As a Supervisor, Clinical Trials Specimen Management at Rochester Regional Health in Rochester, NY, you will be leading a dedicated team responsible for the timely receipt, processing, storage, and shipping of Clinical Trials client specimens. Your role involves supervising employees" performance, supporting the Clinical Trials Specimen Management (CTSM) process, ensuring department turnaround times (TAT), and promoting regulatory compliance, quality assurance, and continuous improvement of CTSM processes. Your responsibilities will include performing all Specimen Management processes with high quality standards, reporting specimen management metrics to support decision-making, supporting ti...
Posted 2 months ago
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