ICON Clinical Research Jobs in Baker

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POSITION SUMMARY Oracle DBA is required to join global DBA team. This is a fast-paced environment and the candidate should be comfortable in working on a number of roles at the same time - as production DBA - supporting and troubleshooting a diverse range of databases and applications; and in a development DBA role working with project teams. Strong technical skills, good documentation habits, and...
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...
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...
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...
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...
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 Messaging-Exchange Engineer III ensures the stability, integrity, and efficient operation of enterprise servers and components and related technologies...
ICON - Be a Part of our Journey. To perform this job successfully, a Network Services Engineer III must be able to perform each essential duty satisfactorily. Documents hardware and software inventory. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essent...
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...
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...
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’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...
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