R & D Jobs in Wheeling, Illinois

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96 Wheeling, IL R & D jobs found on Monster.

Jobs 1 to 20 of 96
Job Title: Senior Manager, Regulatory Affairs CMC - Biologics Position Description This individual is expected to contribute to the development and implementation of CMC regulatory strategy for biologic products in development, with minimal supervision. Coordinate all aspects of CMC regulatory submissions relevant to their assigned projects or programs. Serve as the regulatory CMC representati...
Job Title: Assoc Director, Reg Affairs Strategy - CMC Position Description Independently develops and leads the execution of regulatory CMC development and registration strategies as the RA CMC member on Regulatory, Pharmaceutical Development, and Production project teams for assigned products throughout clinical development and commercial lifecycle Demonstrates leadership and comprehensive und...
Would you like to work as a Technical Writer for a great Pharmaceutical company? Every day, Kelly Scientific Resources connects scientific professionals with opportunities to advance their careers, and we currently have one direct hire opening for a Technical Writer in Northern Illinois. Responsibilities: Design, write, create, maintain and update technical documentation such as protocols, meth...
Clinical Data Manager Are you a seasoned Data Manager with years of Medical Device or Pharma experience? Are you looking for your next data management challenge that directly impacts patient therapies? Then you may be a great fit for the Clinical Data Manager position located in Lake Zurich, IL. My client, a leader in blood transfusion and cell therapies is looking for a Clinical Data Manager to ...
Applications Scientist, Wheeling, IL Kelly Scientific Resources has an immediate opening for a results-oriented Applications Scientist in Wheeling, IL. This is a Temp to Hire position with an established company that offers great benefits and the perk of paying out any unused vacation days. Join the team! Applications Scientist Duties: - Work on dairy and beverage applications, interfacing wit...
Kelly Clinical Research is seeking a Safety Data Coordinator for a contract opportunity in Deerfield, IL. This position is a member of the Safety Operations functional area within Global Pharmacovigilance. This position is responsible for the coordination and data entry of adverse event related information, including duplicate checks within the Global Safety Database. Essential Duties and Respons...
Job Title: Research Study Manager, Global External Research Position Description Manage all aspects of the Global External Research (GER) program for multiple therapeutic areas and product programs, including execution of Phase IV non-registration and Investigator Initiated Sponsored Research studies. Manage TA and product level study budgets and communicate study activities to internal stakehol...
Support all stages of development for Alzheimer's Disease disease programs from the drug discovery stage through product registrations world-wide. Responsible for various aspects and oversight for ongoing clinical trials within the therapeutic area. This activity also includes but is not limited to abstract submission, manuscript preparation, investigator meetings, and Scientific Advisory Boards. ...
Support the identification, investigation, mitigation and communication of drug safety issues applying proactive, data-driven and science-based approaches to pharmacovigilance and working collaboratively and strategically with colleagues in multiple disciplines assess risks in the context of efficacy and patient safety. Activities: *** Leading the scientific elements of pro-active safety evaluat...
Kelly Clinical Research is seeking a Safety Review Specialist for a 1 year contract opportunity with the potential to extend in Deerfield, IL. The Safety Review Specialist is a member of the Safety Operations team within Global Pharmacovigilance and serves as a case owner for adverse events to ensure timely and accurate review, processing, and reporting. Responsibilities: May perform initial tri...
The Information Management Center Analyst is responsible for providing internal clients with business, scientific, technical, and patent research reports and analysis. This individual will monitor developments and proactively communicate regarding content and delivery systems, recommend products for review including seeking client feedback, and assist in the implementation of new products and serv...
Role: Project Managerlocation: Deerfield, ILAssignment Length: 6 months, extensions expected OBJECTIVE: The Project Manager provides project leadership to a diverse number of global, cross- functional teams in the successful delivery of early to last-phase development and implementation of projects or sub projects. These responsibilities include leadership of the team in predicting and planning s...
Seeking M.D., Ph.D., PharmD, or DO and 5+ tears track record as safety leader for pharmaceutical company to assume global safety and pharmacovigilance leadership position involving novel immunological therapeutics. Shall: *** Lead global safety efforts for multiple post marketing drug programs *** Regularly perform signal detection activities. *** Support due diligence activities. *** Partici...
6 Month Contract Position - H1's/Subcontractors will NOT be considered: · The candidate is responsible for the day- to-day sensory and consumer project management as well as sensory panel leadership/management activities for specified categories. · Plans and conducts independent projects, participates in development of project objectives, executes against same, and recommends action plans to imp...
Kelly Clinical Research has exciting opportunity for a Clinical Supply Specialist. This is a contract opportunity in Lake Forest, IL at a sponsor company. This Clinical Supply Specialist will be accountable for managing critical activities associated with Investigational Medicinal Products (IMP) in the specialty pharmaceutical and biologics space for clinical supplies. Responsibilities: Create a...
Trileaf Corporation is a full service environmental, and architecture and engineering consulting firm that assists clients with environmental due diligence, regulatory compliance, and engineering & architectural design. Trileaf serves the real estate, financial, petroleum and wireless industries from its headquarters in St. Louis, MO and branch offices in Chicago, IL; Des Moines, IA; Orlando, FL; ...
The Director, EPO Marketing: Provide commercial and cross-functional leadership for the launch of Hospira's first US biosimilar, EPO. Work closely with teams and business partners in the US to prepare for product launch and in Europe to gain understanding of marketing best practices and tactics. Help to shape the US strategy in an emerging regulatory and competitive landscape. Build foundational c...
Regis Technologies, a growing and privately owned chemical company specializing in bulk pharmaceuticals, has an opening for a Method Development Scientist. Qualified candidates will have a Ph.D. in Chemistry, or equivalent, with 10+ years experience in an analytical laboratory environment and 5+ years experience in method development. Technical duties include development of analytical methods, ass...
Responsibilities: Perform topical formulation (pharmaceutical products) research and development. Prepare and process skin, cornea, or nail samples. Perform skin/cornea/nail 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 accordanc...
The Henry M. Jackson Foundation for the Advancement of Military Medicine Inc. (HJF) is seeking a Clinical Research Coordinator for the Operational Infectious Disease Program located at the Naval Hospital in Great Lakes, IL. HJF provides scientific, technical and programmatic support services to the Operational Infectious Disease Program. Responsibilities: Monitor the medical clinic or sick call ...

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