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Integrated Resources INC

US professional staffing firm specializing in IT, life-sciences and healthcare contract placement.

H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
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https://irionline.com ↗

Correct Integrated Resources INC

Integrated Resources INC is…
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Company facts

Headquarters
United States

About

Integrated Resources, Inc. (IRI) is an American professional staffing firm founded in 1996 and headquartered in Edison, New Jersey. It provides contract, contract-to-hire and direct-hire placement in information technology, clinical research, rehabilitation therapy and nursing for clients across North America.

Open positions

64 jobs
Integrated Resources
4 views 9 years ago

Pharmaceutical - Quality Assurance

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
San Diego, CA

Job Description: The individual in this position is responsible for performing day-to-day quality assurance (QA) activities, managing QA processes such as document management, internal audits, instrumentation change…

Corrective Action GCP
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Integrated Resources
3 views 9 years ago

Bench Scientist I

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Andover, MA

Job Description: Responsible for the lifecycle of regulated and clinical samples of bio therapeutics in various matrices to be tested in ligand binding assays on various instrument platforms. Responsible for the…

GCP LIMS
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Integrated Resources
4 views 9 years ago

Clinical Records Associate

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Foster, CA

Job Description: * Maintain a minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical study records. * Participate in…

GCP
Integrated Resources
4 views 9 years ago

Lead Clinical Research Associate

Open 15d North AmericaLead H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Raritan, NJ

Title: Lead Clinical Research Associate Location: Raritan, NJ 08869 Responsibilities: LEAD CLINICAL RESEARCH ASSOCIATE: Under supervision of Clinical Project Lead, oversees performance of assigned field monitors and…

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Integrated Resources
4 views 9 years ago

Director of Clinical Quality

Open 141d RemoteNorth AmericaLead H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Cambridge, MA

Overview: Candidates may need to travel to investigator sites Candidates can sit remote but need to be able to travel to Cambridge Local candidates preferred but they can work from home occasionally 1 year assignment…

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Integrated Resources
4 views 9 years ago

Clinical Trial Assistant

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Malvern, PA

Job Description: This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines with a specific focus on Temperature…

GCP Process Improvement SharePoint
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Integrated Resources
2 views 9 years ago

Regulatory Affairs Manager III

Open 141d North AmericaContract H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Spring House, PA

The Manager, L&A Non-Portfolio Activities, is responsible for project management support for the BRQC Licensing & Acquisitions Group. This includes but not limited to: maintenance of the L&A Portfolio and Non-Portfolio…

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Integrated Resources
6 views 9 years ago

Clinical Research Scientist

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Woodcliff Lake, NJ

Title: Clinical Research Scientist Duration: 12 Months (Possibility of Extension) Location Woodcliff lake NJ Job Responsibilities: The incumbent is responsible for, but not limited to the following: Assist in the…

GCP
Integrated Resources
1 views 9 years ago

Sr. Clinical Trial Management Associate

Open 141d North AmericaSenior H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Foster City, CA

Title: Sr. Clinical Trials Management Associate Duration: 6 Months Location: Foster City, CA, United States JOB RESPONSIBLITIES AND SKILLS Must meet all requirements for CTMA position and have demonstrated proficiency…

GCP
Integrated Resources
2 views 9 years ago

Technical Writer

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Cambridge, MA

Job Responsibilities: · Prepare and review controlled process documents to ensure submitted procedures are compliant and meet the requirements of R&D document control procedures. · Support Process Owners in the…

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Integrated Resources
4 views 9 years ago

Clinical operations Lead

Open 141d North AmericaLead H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Cambridge, MA

Job Summary: Partners with COLs and/or Study Management Team members to support the development of operationally feasible and clear protocol concepts and final protocols. Leverages phase and operational expertise to…

GCP Process Improvement Risk Assessment
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Integrated Resources
9 years ago

Regulatory Affairs Manager III

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Fort Washington, PA

Develops, maintains, and executes vendor oversight activities for assigned trials / indications to ensure quality in the execution of clinical trials, compliance with regulatory requirements and SOPs, and to ensure a…

GCP Performance Management
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Integrated Resources
4 views 10 years ago

Senior Clinical Study Manager

Open 141d North AmericaSenior H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Woodcliff Lake, NJ

JOB DESCRIPTION: Provide operational leadership for assigned trials executing them on time and within budget Overall coordination and management of clinical trials from startup to closeout Liaise with other functional…

GCP
Integrated Resources
2 views 10 years ago

Clinical Trials Management Associate – II

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Foster City, CA

Must meet all requirements for CTMA position and have demonstrated proficiency in all relevant areas Must be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and…

GCP
Integrated Resources
4 views 10 years ago

Clinical Project Manager

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
South Plainfield, NJ

The Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader. The Clinical Program manager is the first-line administrator within the Clinical Operations group responsible for the…

GCP
Integrated Resources
4 views 10 years ago

Clinical Research Specialist

Open 141d North AmericaContract H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
New Haven, CT

Contractor will need to train onsite for 3 months and then be able to work remote . · Provide product training and support to clinical sites for the pill cam procedure. · Support the randomization process and act as…

GCP
Integrated Resources
1 views 10 years ago

Validation Scientist

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Rochester, NY

Responsibilities: The successful candidate, working as part of a multi-disciplinary team, will be responsible for running and analyzing compliant Medical Device evaluation tests on new clinical chemistry,…

GCP
Integrated Resources
3 views 10 years ago

Lead Clinical Data Manager.

Open 141d North AmericaContractLead H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Lexington, MA

JOB DESCRIPTION: The Clinical Data Manager will have a demonstrated ability to oversee the data management activities across a single clinical program or group of related studies. Provides Data Management leadership…

GCP SAS
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Integrated Resources
2 views 10 years ago

Clinical Research Coordinator

Open 15d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Malvern, PA

Client develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease,…

GCP Process Improvement SharePoint
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Integrated Resources
5 views 10 years ago

Project Manager I (Clinical)

Open 141d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States
Northborough, MA

Job Title: Project Manager I (Clinical) Job Location: Northborough, MA Duration – 12 +Months Client- Sanofi (5831400) Duties: · Manages the Demand for Packaging & Distribution of Investigational Products for…

GCP