ICON Clinical Research Jobs in Apex

Unfortunately, there are currently no ICON Clinical Research jobs available in Apex:

Study Start Up Associate Expert in Informed Consents needed (develop with template, track versions, track completions and versions, communicate with IRB and Sponsor)! Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs? Study Start...
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 Senior SAS Programmer Analysts play a key role within ICON developing and executing execute statistical programs designed to analyze clinical trial information. The Senior SAS Programme...
· Provide leadership to both sponsor based and ICON based projects including coordinating the projects from the start to the completion of all programming as scheduled. Coordinate programming activities across several trials and indications including publication and regulatory submission activities, manage time lines, provide programming oversight and direction to project programmers, and represen...
Manager, Software Testing & Validation Location – Warrington, PA Competitive Compensation Package 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 Manager, Software Testing & Validation plays a key role within ICON’s Medical Imaging D...
"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...
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 Senior Clinical Data Delivery Lead participates in activities as related to the specification, validation and quality assurance of study data deliverables and applies expert experience...
Quality Assurance Auditor II Location- Whitesboro NY. 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 lead internal and external GXP audits and perform QA audits of data and records in order to assure compli...
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...
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...
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...
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....
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...
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