ICON Clinical Research Jobs in Montana

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If you have managerial experience combined with the know-how of hosting client audits to ensure regulatory compliance for Central Laboratories, learn how you can play a key role in leading a team that oversees global and domestic client audits for ICON Central Laboratories which is dedicated exclusively to central laboratory testing and the associate services for clinical trials. About the Senior...
Laboratory Technician II This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Responsible for performing assays on samples for pharmaceutical and chemical companies. Overview of the Role Perform assays for the routine batch analysis of sample...
Quality Assurance Auditor This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The successful candidate will conduct internal and external GXP audits and perform QA audits of data and records in order to assure compliance with ICON or Sponsor...
Are you a strategic process improvement leader with proven experience in lean six sigma methodologies interested to join an industry leading clinical research organization? About Director, Business Process Improvement at ICON: If so, ICON could be the opportunity for you. We are a European led global CRO and are looking for someone who can help drive the business to fulfill our ambitious strategic...
"At ICON, it's our People that set us Apart" Title: Technical Quality Assurance Analyst Location: Farmingdale, NY If you have experience performing assay specific audits combined with the know-how of hosting client audits, learn how you can join ICON Central Laboratories and be responsible for the implementation, execution and strategic reporting of technical quality assurance functions related to...
Project Manager This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The successful candidate will be responsible for the overall direction, coordination, implementation, execution, control and completion of projects ensuring consistency with...
Are you interested to drive client relationships and business processes within DOC’s – ICON’s leading provider of Resourcing Solutions to the Clinical Trials Industry? Operations Manager role within DOC’s: Founded in 1997, DOCS has grown to become the premier staffing provider to the clinical development industry. The company was acquired by ICON plc. in 2007 and was merged with ICON’s existing re...
Multiple
Home Based Clinical Research Associate Travel up to 70% Phase I-IV experience desired Candidate can be based anywhere in the USA Purpose of the Job: •To plan, execute and support clinical site management activities •To ensure the quality and integrity of the data collected in sponsored clinical trials in accordance with the approved protocol, SOPs, ICH/GCP and regulatory requirements •To support t...
ICON - Be a Part of our Journey. This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our IT Project Managers play a key role within ICON and are responsible for the overall coordination, implementation and completion of regional/global cross...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our Clinical Data Coordinator opportunities in the U.S. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutica...
"At ICON, it's our People that set us Apart" Title: Global Validation Analyst Location: Farmingdale, NY If you have working experience in assay validation in a clinical laboratory setting, learn how you join ICON’s Validation team that’s responsible for managing the performance of analytical validations within ICON Central Laboratories (ICL) including but not limited to the review of assays produc...
If you have a background in Clinical Data Management combined with the know-how of managing large clinical trials, learn more about how you can be a part of a Data Management team that offers complete exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries....
If you have HR Advisor experience within a Service Centre environment combined with the know-how of contributing to a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting internal customer needs, learn how you can play a key role in driving improvement to ICON’s HR Service Centre Team. About the HR Advisor role within ICON: • Deliver se...
"At ICON, it's our People that set us Apart" Title: Senior Trial Master File Owner Location: Any US Location If you have extensive end-to-end Clinical Trial process knowledge along with the expertise of ensuring the completeness and accuracy of documentation within a Trial Master File (TMF) system, learn more about how you can be a part of ICON’s Document Management group that’s responsible for ve...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our Data Management Project Management opportunities. In this role you will manage the activities of data management studies and staff in a manner that ensures all timeframes and targets are met to the sponsor's satisfaction and that costs are kept under control. Position overview: • Manage and D...
"At ICON, it's our People that set us Apart" Title: Trial Master File Owner Location: North Wales, PA If you have extensive end-to-end Clinical Trial process knowledge along with the expertise of ensuring the completeness and accuracy of documentation within a Trial Master File (TMF) system, learn more about how you can be a part of ICON’s Document Management group that’s responsible for verifying...
"At ICON, it's our People that set us Apart" Are you interested in assisting in the day-to-day activities of the analytical laboratory including responsibility for developing and performing assays on biological samples from pre-clinical and clinical trials? Scientist I role within ICON: ICON has a strong reputation in our approaches to clinical development. We apply scientific and operational exce...
Title: Senior Trial Master File Owner Location: Any US Location If you have extensive experience interpreting clinical trial protocols for the purpose of establishing and designing documentation requirements for a Trial Master File system, learn more about how you can be a part of ICON’s Document Management group that’s responsible for verifying clinical trial documentation is consistent with the...
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