9 medical assistant health jobs found in North Chicago, IL

Job Title: REMOTE Data Scientist IIIJob Description We are seeking a highly skilled and innovative Data Scientist III to join our dynamic team. This remote position offers the opportunity to work on cutting-edge AI models and contribute significantly to our data-driven projects. The ideal candidate will collaborate with cross-functional teams to design, develop, and deploy AI models tailored to meet our business needs. Responsibilities Collaborate with cross-functional teams to design, develop, and deploy AI models tailored to business needs. Internalize and integrate external AI programs, ensuring compatibility with our systems. Utilize Python, PyTorch, TensorFlow, and other programming languages for developing and refining deep learning models. Research and implement Graphical Neural Network (GNNs) models and contribute to their adaptation for analyzing data. Implement and apply literature and data-driven network integration strategies to infer...

Job Title: Chemist II Job Description We are seeking a dedicated and skilled Chemist II to join our team, responsible for executing laboratory tasks with precision and technical expertise. This role demands the ability to generate precise, reliable, and reproducible data, ensuring compliance with regulatory requirements while maintaining safety and GxP standards. Responsibilities Independently execute assigned laboratory tasks using standard procedures and technical understanding. Document experiments as per regulatory requirements. Demonstrate strong experimental precision and data interpretation skills. Develop protocols for complex tests or experiments with less defined assays. Ensure safety and GxP requirements are met during tasks. Deliver high-quality, precise data in a timely and compliant manner. Apply basic computer skills including word processing, spreadsheets, and instrument-related systems. Present findings of...

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Key Responsibilities Engineer, implement and support cloud services that underpin scientific and R&D related activities. Provide consultation and support for cloud solutions with a focus on best practices and security. Investigate and engineer new technologies focused on containerization and automation to enhance and secure cloud platforms while fostering agility for the business. Specific duties include: Automate...

Job Title: Construction Superintendent Job Description? The successful candidate will be certified and qualified to execute the duties of Site Superintendent, Quality Control Manager (QCM), or Site Safety & Health Officer (SSHO) on Federal Government construction project sites. The role involves acting as the lead on-site representative, managing coordination efforts among federal clients, subcontractors, and vendors to ensure seamless project execution. The candidate will direct all field construction operations, driving timely completion within budget while meeting federal standards for safety and quality. Responsibilities Serve as the primary on-site representative, coordinating efforts among federal clients, subcontractors, and vendors. Direct all field construction operations, ensuring timely completion within budget while maintaining federal safety and quality standards. Establish and uphold rigorous safety protocols in full compliance with EM...

Description Job Description: Responsibilities as applicable: Take part in post-market safety surveillance activities for assigned medical devices and contribute to area projects and objectives. Identify issues and escalate them to the manager as necessary. Conduct medical safety assessments MSA for medical device complaints involving reported adverse events and occasionally technical events. This involves evaluating the seriousness of adverse events determining device relatedness and assessing whether a recurring malfunction could cause or contribute to serious injury or death. Maintain oversight of all incoming MSAs for timely completion to assist in on-time reporting Skills pharmaceutical, clinical research, regulatory Top Skills Details pharmaceutical,clinical research,regulatory Additional Skills & Qualifications Qualifications: BSN Degree or higher with active RN license Minimally 5-7 years of hands-on clinical experience Able to apply clinical knowledge to...

Job Title: REMOTE Lab Tech III Job Description We are seeking a highly skilled Lab Tech III to support our global laboratories in projects related to Laboratory Information Management Systems (LIMS), specifically Thermo SampleManager. This role requires a strong scientific experience and experience in laboratory analysis and quality systems management. Responsibilities Support global laboratories with ongoing projects related to Laboratory Information Management Systems (LIMS), particularly Thermo SampleManager. Interpret laboratory test methods for the calculations and formulas needed to generate results. Compile custom calculation fields in LIMS (SampleManager) necessary for calculating laboratory results in the system. Work with Chromatographic Data Systems (CDS), such as Empower, as a secondary responsibility. Draft documents to serve as guidelines for the laboratory to use in calculations and report results. Follow calculation...

Job Title: Medical Affairs Project ManagerJob Description The Medical Project Office within Medical Program Management seeks a dedicated Medical Affairs Project Manager to consolidate and standardize repeatable activities, ensuring high quality, consistency, accuracy, and efficiency. The role involves providing project management expertise for the successful execution of Medical Affairs advisory boards and symposia, leading through effective collaboration with Medical Affairs Business Owners, Medical Program Managers, Support Teams, and vendors. Responsibilities Provide project management expertise to ensure successful execution of 25-30 programs focused on Advisory Boards, coordinating resources and stakeholders across vendors and internal groups. Manage planning, cost, timeline, scope, and risk management plans, escalating risks as needed. Lead coordination and project management for internal stakeholders and external vendors supporting logistics and content...

Job Title: Regulatory Affairs Associate IJob Description The Regulatory Affairs Associate I is responsible for managing activities related to marketed product variations, focusing on authoring and compiling chemistry manufacturing and control (CMC) sections to ensure timely preparation of submission documents. This role involves coordinating with all functional departments to support regulatory filings. Responsibilities Manage and compile CMC sections of marketed product variations. Partner with RA CMC Project Leads to develop module 3 content and project timelines. Collaborate with diverse functional groups to ensure the file-ability and acceptance of CMC sections. Manage assigned projects to ensure thoroughness, accuracy, and timeliness of CMC dossiers and responses. Conduct review meetings for submission documents. Understand CMC expectations, including CTD content, structural, and formatting requirements. Maintain awareness of and...

Job Title: Clinical Contract Documentation Specialist IIIJob Description The Clinical Contract Documentation Specialist III will be responsible for processing vendor agreements and Clinical Study Agreements (CSA) into the contracting database. This role ensures all auditable documentation required for payment processing is included and maintains system integrity by resolving vendor management issues. The specialist will process monthly electronic data capture invoices for CSAs in clinical trials, verify patient activity for each agreement, and independently investigate and resolve clinical trial vendor or site payment disputes. Responsibilities Ensure compliance with all applicable Corporate and Divisional Policies and Procedures. Demonstrate operational knowledge of SOPs and practices required to effectively process clinical contracts. Audit and perform financial reconciliation of clinical study vendor contracts using various financial systems to summarize...