R & D Jobs in North Chicago, Illinois

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79 North Chicago, IL R & D jobs found on Monster.

Jobs 1 to 20 of 79
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...
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...
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...
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...
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 a Medical Technologist IIIwith one of our important clients. Position Information: Job Title: Medical Technologist III Location: Lake County, IL Duration: 12 Months Compensation: DOE Contact Information: Van...
Hello, We have an urgent requirement for Clinical Project Manager with one of our clients in North Chicago IL 60064. Please go through the job description and if you find it interesting then please send me an updated copy of your resume ASAP or call me at 919 887 6786 EXT. 4083 Title: Clinical Project Manager Location: North Chicago IL 60064 Duration: 6 Months Job Description: · 2-4 years’ e...
Hi, We have an urgent requirement for Clinical Statistician with one of our clients in North Chicago, IL 60064. Please go through the job description and if you find it interesting then please send me an updated copy of your resume ASAP or call me at 919 887 6786 ext. 4083. Job Title: Clinical Statistician Duration: 10+ Months Location:North Chicago, IL 60064 Job Description: · PhD in Statis...
Your Laboratory Technician skills are needed just about anywhere. But is it where you want to go? Imagine working for one of the nation's most respected companies. Making a strategic contribution. Receiving the rewards and recognition you deserve. Whether you are pursuing a contract or permanent placement, Experis knows how and where to get you where you want to go. In this Infrastructure Project...
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...
Your Clinical Research skills are needed just about anywhere. But is it where you want to go? Imagine working for one of the nation's most respected companies. Making a strategic contribution. Receiving the rewards and recognition you deserve. Whether you are pursuing a contract or permanent placement, Experis knows how and where to get you where you want to go. Are you interested? The ideal Clin...
Perform topical formulation (pharmaceutical products) research and development. Prepare and process skin, cornea, or nail samples. Perform skin/cornea/nail tissue absorption and penetration screening assay. Formulate topical dosage forms including but not limited to: gels, lotions, creams, ointments, solutions, etc. Document laboratory work and prepare project report. Work in accordance with estab...
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...
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...
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...
Job Title: Regulatory Affairs Associate III Position Description Provides regulatory affairs support and expertise by preparing drug and device registration packages for FDA product listings and documentation to facilitate the importation of product into the US. Serves as a lead regulatory representative for assigned project teams. Supports US drug shortage management. Support global device r...
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...
This epidemiology role has responsibility for epidemiologic assessments for emerging safety issues for drugs, therapeutic biologics and vaccines. This role will utilize a variety safety data (spontaneous, clinical trial, pre-clinical, and other relevant information) for the analysis of emerging safety concerns and will participate in the design, conduct and analysis post marketing safety studies. ...
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: 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...

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