integratedresourcesinc

Quality Assurance – Clinical I

The primary responsibility for Groton site based contractor role will be interpreting data and performing quality control activities for ensuring accuracy of the data that is transferred between Client and Vendors with…

QUALITY ENGINEER

Responsibilities: • Serve as a multi-functional team member establishing quality requirements and providing guidance for sustaining engineering projects. • Lead or support Risk Management (in accordance with 18014971)…

Regulatory Compliance

Clinical Database Analyst

POSITION SUMMARY: Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group and for the medical reviewers in the iDARTs application (an internally developed tool…

Data Visualization SAS

Clinical data Manager

Data Quality Vendor Management

1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) Communication with…

IT Customer Support Representative

Position: IT Customer Support Representative Duration: 1 Year Location: Painted Post, NY Hours: Monday - Friday 3:00 PM to Midnight (00:00 AM) ***Bilingual Spanish/English language required*** Verbal & Written Job…

Service Desk

HUMAN RESOURCE COORDINATOR

• Creation of reqs in our Taleo applicant tracking system • Handles new hire paperwork and onboarding processes • Processes termination paperwork • Assists with new-employee orientations. • Completes Forms I-9,…

Corrective Action

Regulatory Affairs Manager III

GCP Networking Risk Assessment

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…

QA Specialist - Formulation

Candidates should have exp with tablets and capsule formulations, clinical products stage I - III, working with contract manufacturing organizations, they are a virtual company so the candidate will give documentation…

Corrective Action

Project Manager

Microsoft Project Process Improvement SharePoint

Duration- 24 months+ Job Description: Actual Title: QA/RA Project Manager (EU MDR) This position will be responsible for project management for programs with regulatory consequences and significant cross functional…

Drug Safety Associate I

Responsible for the receipt and data entry of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide…

Regulatory Compliance

Clinical Research Scientist

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

Laboratory Technician

Seeking a Lab Technician with a primary focus on performing extractions, assisting with sample preparations, and lab maintenance activities such as glassware cleaning, hazardous waste disposal, and order receipt. A…

Hazardous Waste

IT Desktop Support

Job Title:c/Telephony Analyst Duration: 4+ Months Location: Painted post, NY · Operations team member involved in the design and deployment of Cisco Call Manager solutions and IPT Deployments · Perform analysis and…

Cisco Unity

Program Coordinator, Regulatory Information Manager

This role will be coordinating work across 2 major initiatives. One set of work will be tied to approach to IDMP (Identification of Medicinal Products), and the activities specifically tied to the introduction of the…

North AmericaContractSenior

Sr. Programmer Analyst (AS/400)

Position: Sr. Programmer Analyst (AS/400) Duration: 3 Months Location: Maryland Heights MO 63043 Requirements/Certifications: Bachelor's degree 10+ years of experience of programming & analysis in an AS/400…

Clinical Project Manager III

Title: Clinical Project Manager III Location: Lexington, MA, United States Duration: 06+ Months Job Details: • Responsible for the planning, implementation, execution and management of one or more complex clinical…

Data Quality

QA Documentation Specialist-I

Corrective Action Root Cause Analysis

Job Title: QA Documentation Specialist-I Duration: 6 Months Location: Foster City, 94404 Responsibilities: Specializing in compliance and regulatory affairs in the pharmaceuticals & biologics sectors. Meticulous…

North AmericaContractSenior

Sr. Clinical Trial Management Associate

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

Primary Care Services Project Manager