Position Summary: The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials. The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams The role may require providing inputs to design of CRFs, Data Transfer specifications, creation of SDTM specifications and datasets, and reporting the results of clinical trials, including programming rules and electronic submissions for Client`s products. Job-Specific Competencies: 1. Tackles difficult problems; identifies solutions and recommends action management 2. Influences communication toward common understanding and actionable results; 3. Good oral and written communication skills.

Location : Richland WA 99354 The Consultant / Subject Matter Expert (SME) provides strategic guidance and expert advisory support in project management and project controls. This role partners with leadership and key stakeholders to define methodologies, monitor project performance, and ensure large-scale projects are delivered on time, within budget, and aligned with organizational standards and best practices.

Location: Nutley NJ 07110 (Hybrid in the office on Tues, Wed and Thurs) Job Description: The Senior Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners. He/she will respond to medical inquiries, contribute to the development of high-quality Medical Information deliverables, and will be responsible for scientific accuracy review of assigned promotional and scientific exchange materials.

Location : South San Francisco CA USA 94080 The primary responsibilities of the Biophysical Assay Research Associate will include performing analytical method development and testing samples using Capillary Electrophoresis, SDS-PAGE, DLS, MALS, AUC, and other analytical tools; contributing to design and performing experiments with supervision as needed; completing assigned tasks within time frames with high quality; maintaining a well-documented record of activities in lab notebook and reports. The position level will commensurate with education and experience level. Additionally, the role includes regularly summarizing and presenting experimental results in lab meetings and responsible for generating reports. This role will be at our South San Francisco location.

Location : Tucson, AZ 85755 (Onsite) Job summary: Responsible for the coordination and administrative support of key tasks critical to the successful execution of the Facilities & Site Services (F&SS) charter by: Working directly with all internal functional areas located on the Tucson campus to coordinate equipment maintenance. Interacting with external providers to assist in the coordination, execution & organization of maintenance services. Providing administrative support to Facilities & Site Services management staff. Qualifications: To perform this job successfully, an individual must be able to perform each responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the responsibilities.

Location (mandatory): Franklin, TN Tariff Classification & Technical Research: Assign accurate HTS/Schedule B classifications for complex parts by researching engineering drawings and technical specifications to ensure full regulatory compliance. Compliance Auditing & Risk Mitigation: Conduct regular internal audits to identify compliance gaps, manage prior disclosures, and develop long-term process improvements to minimize financial and legal risks. Trade Legislation & Strategic Analysis: Monitor and analyze international trade laws and legislative changes (such as Section 301 or USMCA eligibility) to forecast economic impacts on company operations and supply chain flow. Cross-Functional Collaboration: Act as a central liaison between legal, finance, and supply chain teams to ensure trade strategies and compliance protocols align with broader corporate business goals. Executive Reporting & Decision Support: Synthesize technical trade data into high-level briefings and KPI reports for senior leadership to drive data-driven decisions regarding market entry and cost-saving opportunities. Operational Liaison: Coordinate directly with customs brokers, freight forwarders, and government agencies like CBP to resolve daily documentation discrepancies and shipment delays.

Location:- Morristown, NJ Hybrid Role Internal Title: Learning Business Partner

Location:- Tucson, AZ 85755 (Onsite) Responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support Ventana projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols and quantitative analyses. Presents and discusses results of experiments within department and project team. Maintains high level of professional expertise through familiarity with scientific literature and may participate in conferences and professional societies. Follows company policies and procedures for GMP, GLP, Design Control and others as appropriate. Maintains complete and accurate laboratory documentation and electronic files. May act as principal investigator in conducting own experiments.

Location:- Pearl River NY 10965 This is a laboratory-based position within the Vaccines Early Bioprocess Analytical Development group. The individual will perform routine sample testing, analytical method development and assay qualification studies in support of early vaccine development. Assays include but are not limited to enzyme-linked immunosorbent assays (ELISAs) and other plate-based testing. This is a dynamic position that will require work on fast-moving and high-visibility projects.