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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
6 views 11 years ago

Clinical Site Relationship 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
Cambridge, MA

Job Title: Site Relationship Manager Location: Cambridge, MA Duration: 3 Year+ (Possible Ext.) Job Responsibilities: The Site Relationship Manager (SRM) within Value Based Medicine (VBM) will be responsible for the…

Corrective Action GCP Risk Assessment
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Integrated Resources
9 views 11 years ago

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

Overview- Responsible for the success of the global drug development, manufacturing, clinical trials; coordinates the operational aspects of ongoing global clinical trials to ensure meeting all required timelines as…

GCP Technical Writing Vendor Management
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Integrated Resources
3 views 11 years ago

Clinical Safety Data Manager

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
Cambridge, MA

Primary Duties The Manager, Safety Data Collection, Clinical Trials is responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval Clinical Studies globally. The employee supports the Senior…

GCP Performance Management
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Integrated Resources
4 views 11 years ago

Clinical Trials Safety Data Manager

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
Cambridge, MA

Client: Direct Client Location: Cambridge, MA Job Title: Safety Data Collection Manager Duration: 1 year Responsibilities • Responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval…

GCP Performance Management
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Integrated Resources
8 views 11 years ago

Clinical Research Coordinator

Open 15d North AmericaInternship 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 York, NY

• The Clinical and Research Collaboration (CRC) Liaison has primary responsibility for the oversight and management of clinical and research collaborations within assigned Therapeutic Area(s) • Clinical and research…

Analytics GCP
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Integrated Resources
7 views 11 years ago

Statistical Programmer

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
East Hanover, NJ

Candidate to develop standard global data review tools, such as patient profiles, data quality checks, exception reports, PD reports, listings and figures for oncology trials. Ensure timelines and adequate quality of…

Data Quality GCP SAS Statistics
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Integrated Resources
3 views 11 years ago

Quality 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
Groton, CT

• To work with and on behalf of CTPQ/GCP Compliance Management within DevOps, performing management Significant Quality Events. • Significant Quality Event Lead: the individual responsible for the formation and leading…

DevOps GCP Process Improvement Root Cause Analysis
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Integrated Resources
8 views 11 years ago

Clinical Safety Data Manager

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
Cambridge, MA

• The Manager, Safety Data Collection, Clinical Trials is responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval Clinical Studies globally. The employee supports the Senior Manager,…

GCP Performance Management Technical Writing
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Integrated Resources
2 views 11 years ago

Sr.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

• This role focuses on phase 4 work and requires solid experience with multiple phase 4 studies. • Partners with Medical Research and other functions to develop operationally feasible and clear protocol concepts and…

GCP Risk Assessment Vendor Management
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Integrated Resources
2 views 11 years ago

Associate Director (Trial Master File)

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

DIRECT CLIENT NEED – Immediate interview!!! Position: Associate Director (Trial Master File Operations and Systems Management) Location: Cambridge MA Duration: 6+ Months Responsibilities: • Manage overall TMF…

GCP Vendor Management
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Integrated Resources
2 views 11 years ago

Clinical Documentation Specialist

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
Lexington, MA

Title: Clinical Documentation Specialist Location: Lexington, MA Duration: 6 months (possible extension) JOB SUMMARY: • Manages the Trial Master Files (all of the documents that support the clinical trials-everything…

GCP
Integrated Resources
3 views 11 years ago

Senior Clinical Study Manager

Open 141d North AmericaContractSenior 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

OBJECTIVE: Execution of clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and Takeda SOPs, and supporting clinical strategy defined in…

GCP
Integrated Resources
2 views 11 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

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 and expertise to…

GCP SAS
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Integrated Resources
2 views 11 years ago

Pharmacist

Open 15d North AmericaFellowship 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

Location: New Haven, CT Duration: 1 year+ The Pharmacist provides operational pharmacy support, under the direction of the Head of Pharmacy, at a clinical development stage biopharmaceutical company. The Pharmacist…

GCP
Integrated Resources
4 views 12 years ago

Clinical Study Manager

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
Cambridge, MA

1. Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and SOPs, and supporting clinical strategy defined in Clinical Study Plan (CSP).…

GCP
Integrated Resources
2 views 12 years ago

Senior Clinical Study Manager

Open 141d North AmericaContractSenior 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

1. Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and Takeda SOPs, and supporting clinical strategy defined in Clinical Study Plan…

GCP
Integrated Resources
2 views 12 years ago

Sr. Clinical Study Manager

Open 141d North AmericaContractSenior 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

Sr. Clinical Study manager Job Description: Execution of clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and SOPs, and supporting clinical…

GCP
400K – 150M $
Integrated Resources
2 views 12 years ago

Clinical Project Scientist

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
Raritan, NJ

RESPONSIBILITIES: Clinical Project Scientist - Cardiovascular Metabolism (CVM) Medical Affairs The Clinical Project Scientist (CPS) is a key interface role in the CVM Medical Affairs (CVM MA) organization responsible…

GCP
Integrated Resources
4 views 12 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 Description: • Partners with Medical Research and other functions to develop operationally feasible and clear protocol concepts and final protocols. • Leverage Phase and operational expertise to establish study…

GCP Risk Assessment Vendor Management
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Integrated Resources
2 views 12 years ago

QA Manager

Open 140d 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
East Windsor, NJ

Job Requirement • Create and Establish a scientific approach to the company quality and regulatory system. • Ensure all GMP, GLP, GCP operations are in compliance , • Establish training and audit programs, as well as…

GCP