- job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clinjob summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
- job summary: Support the rigorous evaluation of positron emission tomography (PET) radiotracers using in vitro radiopharmacology techniques. location: North Chicago, Illinois job type: Contract salary: $30.00 - 35.89 per hour work hours: 9 to 5 education: Bachelors responsibilities: Conduct reproducible experiments that evaluate the interaction of radioactive small molecule ligands with their target proteins, including sample preparatiojob summary: Support the rigorous evaluation of positron emission tomography (PET) radiotracers using in vitro radiopharmacology techniques. location: North Chicago, Illinois job type: Contract salary: $30.00 - 35.89 per hour work hours: 9 to 5 education: Bachelors responsibilities: Conduct reproducible experiments that evaluate the interaction of radioactive small molecule ligands with their target proteins, including sample preparatio
- job summary: One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: North Chicago, Illinois job type:job summary: One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: North Chicago, Illinois job type:
- job summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1stjob summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1st
- job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Preparejob summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare
- job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatmentjob summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
