Shift details: Hours could be anytime between 6am and 10pm (usually 8-hour shift).Mon-Friday - 8-hour shift. Shifts will be in increments of 8.5 hrs. with 30min lunch and can vary from 7am to 7:30pm i.e., 7-3:30, 9-5:30, 11-7:30 Over time ...
Job Description: Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results. Interprets data output to deter...
Job Description: Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results. Interprets data output to deter...
Job Description: The Senior Engineer position within the Science and Technology (S&T) organization is responsible for the development, improvement, and verification of electro-mechanical medical devices. This technical expert will, with li...
Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS), uploading documents, Qin documents uploaded to ensure accurate categorization. Track CTIS application details to compile metric...
Responsibilities: Independently identify, prioritize, and lead all CDM activities for assigned study. Represent CDM function at internal/external team calls. Communicate and able to provide CDM expertise for DM related activities. Resp...
Responsibilities: Support Digital Strategy Lead in the development of digital strategy and Client endpoint and provide input in the patient insight research, technologies evaluation, usability testing, vendor qualification, and validation...
Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental proced...
Job Description: The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing, designing, and implementing high-priority analytical strategies, clinical oversight, and initiatives. The team is...
Responsibilities: Collect, assess, and process adverse event information (both clinical and post-marketing) in a compliant and timely manner to adhere to global regulations. Seriousness assessment. Labelling. Causality determination. ...
Responsibilities: Responsible for providing guidance to ensure that all regulatory submissions are planned, communicated, and performed per regulatory and business requirements. In addition, this position serves as a subject matter expert...
Job description: This position provides support and drive for activities that support the overall long-range plan ensuring the department/functions continues to be competitive and meets all required cost, compliance and customer service ne...
Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best p...
Responsibilities: Technical expert that will independently investigate, identify, develop, and optimize new methods/ techniques to address critical project needs. Continuously seek to improve existing laboratory methods and processes. R...
Responsibilities: Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting. Develop and manage data management timelines for multiple projects, ensuring all milestones...
Responsibilities: The candidate will have the opportunity to develop and advance AI/ML technologies at the heart of computer-aided drug design. The candidate should have broad experience with computational techniques with a focus on stru...
Job Description: Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results. Interprets data output to deter...
Job Description: Quantitative, Translational & ADME Sciences Department has an open position for a Scientist III position in North Chicago, IL. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysi...
Job Description: The Project Manager (Contractor), Office of Integrations & Acquisitions (OOIA) reports through Clinical Sciences, Strategic Operations, and is responsible for driving high-impact, cross-functional projects across Clinical ...
Responsibilities: The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials. This role is key to implementing programming standards an...