ICON Clinical Research Jobs in Montana

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Manager, Study Conduct 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. You will be responsible for the overall direction and management of projects through designated Study Manager I, Clinical Research Coordinator and Research Assistants...
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...
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...
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...
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...
"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...
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...
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...
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....
Title: Trial Master File Owner Location: North Wales, PA If you have 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 TMF specification...
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 product inserts, preparation of validation plans, identification and attainment of suitable samples for valida...
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...
Title: Project Manager, Imaging Clinical Trials Location: Warrington, PA If you have a background as an Imaging Technologist combined with the know-how of managing large clinical trials, learn more about how you can be a part of a Medical Imaging team that offers complete solutions for clinical trials that require the acquisition, collection, management and analysis of global medical image data. A...
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...
If you’re a Medical Technologist with Molecular Diagnostic and/or Nucleic Acid preparation experience learn more about how you can be a vital part of ICON Central Laboratories which is dedicated exclusively to central laboratory testing and the associate services for clinical trials. About the Medical Technologist role within ICON: The Medical Technologist will be responsible for performing techni...
Are you an effective manager with a passion to lead ICON’s global laboratory quality assurance team and build organizational structure and processes around compliance? About Senior Director, Laboratory Quality Assurance at ICON: ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical tria...
"At ICON, it's our People that set us Apart" Are you interested in joining a respected proposals team that has been recognized for strong leadership, collaboration, quality, and dependability within a fast paced, deadline-driven environment? ICON’s Early Phase proposals team is comprised of high performing professionals who take pride in delivering timely, client-focused proposals for clinical pha...
"At ICON, it's our People that set us Apart" Title: Quality Assurance Auditor Location: Farmingdale, NY Are you a Quality Assurance Auditor with extensive experience assessing the compliance of Laboratory Facilities and ISO quality standards in the State of New York? If so, learn more about how you can be a part of a team that manages client audits for ICON Central Laboratories which is dedicated...
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 Clinical Trial Assistants (CTA’s) play a key role within ICON. Working closely with our global clinical teams the Clinical Trial and Project Managers to...
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