Knowledgeable in the implementation and workings of IRT systems * Ability to create a collaborative environment and manage multiple project activities * Strong computer skills including MS Office
Knowledgeable in the implementation and workings of IRT systems * Ability to create a collaborative environment and manage multiple project activities * Strong computer skills including MS Office
IRT & Fabrication Coordinator
Brea, CA · On-site
... fuel projects. Job Summary Shambaugh & Son is seeking an IRT & Fabrication Coordinator. In this ... role you will be responsible for coordinating the completion of material requests, fabrication ...
IRT & Fabrication Coordinator
Brea, CA · On-site
... fuel projects. Job Summary Shambaugh & Son is seeking an IRT & Fabrication Coordinator. In this ... role you will be responsible for coordinating the completion of material requests, fabrication ...
Project Manager - RTSM (Remote)
New York, NY · On-site +1
$84K/yr
The Project Manager - RTSM is responsible for the overall relationship management of RTSM client ... IRT and a solid understanding of Clinical Research SaaS technology * Excellent verbal/written ...
Project Manager - RTSM (Remote)
New York, NY · On-site +1
$84K/yr
The Project Manager - RTSM is responsible for the overall relationship management of RTSM client ... IRT and a solid understanding of Clinical Research SaaS technology * Excellent verbal/written ...
Project Manager - RTSM (Remote)
New York, NY · On-site +1
$84K/yr
The Project Manager - RTSM is responsible for the overall relationship management of RTSM client ... IRT and a solid understanding of Clinical Research SaaS technology * Excellent verbal/written ...
Project Manager - RTSM (Remote)
New York, NY · On-site +1
$84K/yr
The Project Manager - RTSM is responsible for the overall relationship management of RTSM client ... IRT and a solid understanding of Clinical Research SaaS technology * Excellent verbal/written ...
RTSM/IRT services delivery and eClinical systems implementation. * Software implementation and testing experience required in clinical research or supply chain related industry. * Project management ...
RTSM/IRT services delivery and eClinical systems implementation. * Software implementation and testing experience required in clinical research or supply chain related industry. * Project management ...
Project Manager - eCOA
Malvern, PA · On-site
The eCOA Project Manager will lead project planning and execution, ensuring timely delivery and ... YPrime simplifies clinical trials with eCOA, IRT, and eConsent solutions that combine speed ...
Project Manager - eCOA
Malvern, PA · On-site
The eCOA Project Manager will lead project planning and execution, ensuring timely delivery and ... YPrime simplifies clinical trials with eCOA, IRT, and eConsent solutions that combine speed ...
Experience implementing IxRS/IRT, ePRO, and eCOA systems * Strong project management and vendor oversight experience * Working knowledge of Good Clinical Practices (GCP) and FDA regulations
Quick apply
Experience implementing IxRS/IRT, ePRO, and eCOA systems * Strong project management and vendor oversight experience * Working knowledge of Good Clinical Practices (GCP) and FDA regulations
Preferred US location is East coast The Study Project Lead will lead client support of the ... Identify opportunities to improve the study IRT, product, or support processes to reduce support ...
Preferred US location is East coast The Study Project Lead will lead client support of the ... Identify opportunities to improve the study IRT, product, or support processes to reduce support ...
Manage IRT system setup and maintenance, including drug assignment logic, inventory thresholds, and ... Collaborate cross-functionally with Clinical Operations, QA, Regulatory, and Project Management to ...
Manage IRT system setup and maintenance, including drug assignment logic, inventory thresholds, and ... Collaborate cross-functionally with Clinical Operations, QA, Regulatory, and Project Management to ...
Client Services Project Manager
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... Technology (IRT) Req Equivalent combination of education, training and experience Req Strong ...
Client Services Project Manager
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... Technology (IRT) Req Equivalent combination of education, training and experience Req Strong ...
Client Services Project Manager
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... Technology (IRT) Req Equivalent combination of education, training and experience Req Strong ...
Client Services Project Manager
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... Technology (IRT) Req Equivalent combination of education, training and experience Req Strong ...
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Quick apply
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Study Project Manager (Medical Affairs/Immunology/Oncology)
$148K - $202.50K/yr
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Study Project Manager (Medical Affairs/Immunology/Oncology)
$148K - $202.50K/yr
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Study Project Manager (Medical Affairs/Immunology/Oncology)
Mettawa, IL · On-site
$148K - $202.50K/yr
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Study Project Manager (Medical Affairs/Immunology/Oncology)
Mettawa, IL · On-site
$148K - $202.50K/yr
Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. * Manage IP & study supplies. Support process improvement ...
Client Services Project Manager
Durham, NC · On-site
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... IRT) Req • Equivalent combination of education, training and experience Req • Strong ...
Client Services Project Manager
Durham, NC · On-site
$57K - $142.60K/yr
Will ensure that all project work is completed in accordance with SOPs, policies and practices ... IRT) Req • Equivalent combination of education, training and experience Req • Strong ...
Senior Manager, Global Supply Chain
Waltham, MA · On-site
$143K - $175K/yr
Knowledgeable in the implementation and workings of IRT systems * Ability to create a collaborative environment and manage multiple project activities * Strong computer skills including MS Office
Senior Manager, Global Supply Chain
Waltham, MA · On-site
$143K - $175K/yr
Knowledgeable in the implementation and workings of IRT systems * Ability to create a collaborative environment and manage multiple project activities * Strong computer skills including MS Office
Director, Academic Technology Services
Sacramento, CA · On-site
$16.22K/mo
This position has a strategic focus on supporting academic technology and CSU System Accessible Technology Initiatives (ATI) related projects and services offered by IRT. Additionally, this position ...
Director, Academic Technology Services
Sacramento, CA · On-site
$16.22K/mo
This position has a strategic focus on supporting academic technology and CSU System Accessible Technology Initiatives (ATI) related projects and services offered by IRT. Additionally, this position ...
Collaborate with PCI Packaging Project Manager (PM) to establish a production schedule based on the ... Participate in IRT Requirements gathering process and provide input for IRT specification documents
Collaborate with PCI Packaging Project Manager (PM) to establish a production schedule based on the ... Participate in IRT Requirements gathering process and provide input for IRT specification documents
Director, Academic Technology Services
Sacramento, CA · On-site
$16.22K/mo
This position has a strategic focus on supporting academic technology and CSU System Accessible Technology Initiatives (ATI) related projects and services offered by IRT. Additionally, this position ...
Director, Academic Technology Services
Sacramento, CA · On-site
$16.22K/mo
This position has a strategic focus on supporting academic technology and CSU System Accessible Technology Initiatives (ATI) related projects and services offered by IRT. Additionally, this position ...
Function as clinical supply point person on cross functional projects to identify and escalate supply risks. * Provides input to IRT specification design. Reviews assigned IRT threshold levels to ...
Function as clinical supply point person on cross functional projects to identify and escalate supply risks. * Provides input to IRT specification design. Reviews assigned IRT threshold levels to ...
Irt Project information
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$14.42 - $17.77
16% of jobs
$20.20 is the 25th percentile. Wages below this are outliers.
$17.77 - $21.11
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9% of jobs
The median wage is $27.13 / hr.
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8% of jobs
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8% of jobs
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3% of jobs
$44.51 - $47.86
3% of jobs
$47.86 - $51.20
2% of jobs
$14
$30
$51
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Posted 22 days ago
Job description
What You'll Do:
The Senior Manager, Global Supply Chain reports to the Associate Director, Global Supply Chain and possesses a strong proficiency in clinical supply management and project management practices. The Senior Manager, Global Supply Chain will support the Associate Director, Global Supply Chain to ensure uninterrupted supply of Investigational Medicinal Product (IMP) for clinical studies as well as inventory of comparator drug products (if applicable).
Required location: Waltham, MA (hub-based, onsite 3-4 days per week)
Responsibilities:
- Supporting investigational drug product supply and logistics activities, including, but not limited to, demand forecasting and supply planning, IRT start-up and maintenance, label development and proof generation, packaging and labeling operations, release, distribution, expiry extension, pharmacy manual development, returns, reconciliation, destruction, and inventory management
- Support oversight in monitoring inventory levels throughout the life of a clinical trial
- Supporting oversight of packaging and labeling/distribution vendors, including relationship management
- Interpret clinical synopses and protocols to create clinical IMP demand forecasts
- Attend clinical study and cross functional meetings as needed
- Support global supply chain lead in overseeing the execution of multiple clinical trials and proactively identify potential supply chain issues, and recommend solutions to global supply chain lead
- Support clinical study close-out activities, including returned goods reconciliation and inventory destruction
- Assist with change controls and deviations as needed
- Support temperature excursion processes as required
- Support the IRT System Leads as necessary with regards to user requirement specifications and management module(s) as applicable
Required Qualifications:
- Experience managing clinical supplies for late phase, global clinical trials
- 8+ years of relevant biopharmaceutical industry experience with 5+ years in clinical supply management
- Knowledgeable in the implementation and workings of IRT systems
- Ability to create a collaborative environment and manage multiple project activities
- Strong computer skills including MS Office
- Hands-on, roll-up-your-sleeves, collaborative approach with high sense of urgency and drive for results
- Ability to think outside of the box and challenge the status quo
- Desire to work in a fast-paced, innovative environment
Education:
- Bachelor's degree in pharmaceutical science, engineering, life sciences, or another relevant field. Advanced degree preferred