R & D Jobs in Lake Forest, Illinois

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81 Lake Forest, IL R & D jobs found on Monster.

Jobs 1 to 20 of 81
Summary: The Sr. Regulatory Affairs Associate provides regulatory support and expertise by developing global regulatory strategies, identifying needed registration data, obtaining this data and ensuring that it is effectively presented for the registration of products. The Sr. Regulatory Affairs Associate may serve as a lead regulatory representative to an assigned product or project team. Major...
ATR International has been a leader in the staffing industry since 1988, placing professionals in the industry's most innovative companies. We currently have an exciting opportunity for an Associate Scientist I with one of our important clients. Position Information: Job Title: Associate Scientist I Location: Lake County, IL Duration: 12 Months Compensation: DOE Contact Information: Andrew ...
6 Month Contract Positions: · The candidate will contribute to the preparation of regulatory filing documents and other technical documents through authoring and verification of the documents. · The candidate should have sound technical writing skills, verification skills, strong understanding of scientific concepts. · Must be self-motivated and demonstrate strong initiative. · A scientific ba...
Job Title: Global Regulatory Affairs Intelligence Manager Position Description Ensures appropriate execution of a global regulatory intelligence program for global regulatory affairs. The regulatory intelligence program consists of researching, analyzing, interpreting, communicating and acting on publicly available regulatory information to drive compliance, shape future regulations and guidelin...
Job Title: Regulatory Affairs Strategy Associate Position Description Executes regulatory activities for team members or projects in accordance with applicable regulations and guidelines under supervision. Prepares, review and releases NDA annual reports and required submissions to INDs such as investigator updates, safety reports, and annual reports, as well as assistance in preparation of IND...
LCR HALLCREST is an International Leader in Thermometry, Graphics, Packaging and Specialty Items That Change Color When Exposed to Environmental Fluctuations. Production Laboratory Technician - Job summary This position requires the qualified candidate to perform various duties to support the daily operations of the Production Laboratory. Responsibilities include but are not limited to: Manufa...
The Regional Scientific Manager, Health Outcomes & Pharmacoeconomics (HOPE), is a field-based health outcomes liaison position within Medical Affairs, responsible for developing and fostering key relationships, supporting medical affairs strategies, and advancing the scientific knowledge and value messaging of Hospira's biosimilar portfolio to select Key Opinion Leaders (KOLs), payer decision make...
Oversee the overall operational direction of the global GPS Drug Team. Primary point of contact for all drug operations and liaison between the GPS Drug Team and senior management. Responsible for the Quality and timeliness of regulatory adverse event reporting. Provide training, assistance, guidance, and mentoring to GPS drug team members, evaluate performance, and provide feedback. Establish ...
The Project Manger of Clinical Supplies is responsible for forecasting, coordinating and managing the packaging, labeling, distribution and destruction of clinical supplies for US and ex-US clinical trials. The individual provides technical expertise and leadership to project teams to develop budgets and timelines for multiple clinical programs at a time . 1. Responsible for scheduling, coordinat...
Technical expert in a discipline important to Hospira and an innovator of new products. Demonstrated ability to solve complex technical problems through analytical solutions. Performs activities as an individual contributor or as a part of a project or microbiology team where necessary. Attends external technical meetings and contributes to scientific publications. Write, coordinate and review te...
The director of Global Public Affairs is primarily responsible for managing the development and execution of the company's biosimilars communications programs, with a focus on global public relations strategies to support Hospira's top 3 biosimilars business. Priority responsibilities include working with global and regional leaders to develop and execute communications strategies to amplify and a...
The Calibration department is primarily responsible for: 1. The coordination of the Lake County Calibration Program ensuring all instruments calibration status' are current and ensuring calibration related procedures meet Corporate policy 2. Providing calibration, troubleshooting and repair services of instruments in Lake County, Pleasant Prairie, Distribution Centers and Field Service. 3. The ...
Job Title: Project Manager – Clinical Research Position Responsibilities Manage and develop project team. Supervise and evaluate assigned project staff activities and job performance. Provide continuous support of monitoring responsibilities. Develop protocol monitoring guidelines and other assorted project-specific training instructions. Act as principle liaison between sponsor, CRO (Clinic...
Job Title: Specialist, Regulatory Affairs Position Description Compiles all materials required for submissions, license renewal and annual registration Demonstrative experience with Trackwise and SAP, highly desirable Advanced experience with Microsoft Office Applications is a must The ability to work under pressure, be self-directed, excellent attention to detail and adhere to strict deadlin...
Good Day, We have an urgent requirement for Medical Reviewer/Safety Reviewer at North Chicago IL 60064 with one of our clients. Please go through the job description and if you will find it interesting then send me an updated copy of your resume or you can call me at 919-887-6786 Ext 4083 Position: Medical Reviewer/Safety Reviewer Location: North Chicago IL 60064 Duration: 24+ months Descript...
Primary job function: The primary function of the Safety Coder is to ensure accurate and consistent coding of medical data including, but not limited to, adverse event verbatim descriptions and medication terms received from global clinical trials across all therapeutic areas. Job responsibilities: Prepares coding assignments for new studies and collaborates with clinical team representatives o...
Job Title: US Medical Affairs Study Manager Position Description Provides oversight of Clinical Study Manager and study conduct ensuring studies are conducted according to the Code of federal Regulations, Good Clinical Practices, ICH Guidelines, local regulatory requirements and company SOPs. Oversight of study development and conduct in alignment with company SOPs, and assist with documentatio...
Job Title: Sr. Information Specialist Position Description The (Sr.) Information specialist responds to requests for information by assigned, global Company stakeholder groups and with database searching, alerting services and training in the optimal use of Knowledge & Information Center (KIC) resources. This role partners with internal stakeholders in all regions and functional areas in the id...
Job Title: Clinical Research Associate II Position Description Manager is looking for candidates with broad experience, rather than specific to monitoring Experience writing protocols and final reports is required Experience managing all aspects of a clinical trial is required Position Responsibilities Conduct clinical research throughout all stages of a project, including design, implementa...
Summary: Assures that new products are developed in line with the global registration requirements of targeted countries and obtains expedient registration of these products in a cost effective manner. Maintains registrations of existing products in compliance with applicable regulations. Major Duties and Responsibilities: Develops regulatory strategies for development projects and manufacturin...

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