The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requi...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
Supervises all PMO staff including project managers and domain leads. Provides oversight for all projects. Standardizes methodologies and processes for project management. Encourages skill development of project team members. ...
Supervises all PMO staff including project managers and domain leads. Provides oversight for all projects. Standardizes methodologies and processes for project management. Encourages skill development of project team members. ...
Product Data Engineering Analyst will lead the control and management of engineering design data including the Engineering Change Management process. Senior Product Data Engineering Analyst. Audit the product data in SAP to guarantee the integrity of the data. Will be responsible for the establishme...
Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP / ICH and country clinical research law and guidelines. The Senior Clinical Research Associate is responsible for the following:. Performs clinical study site management/monitoring activities i...
The Data Analyst will act as a Product Owner responsible for Data Ingestion activities and manage the prioritization of backlog items for the team. Experience with Data and Analytics teams who may be working on data consumption (dashboard / analytics) related activities. Experience with data visuali...
This individual should have Federal and Commercial Project Management construction experience that will allow them to successfully manage multiple projects, hold preconstruction meetings and complete projects according to client requirements. Project Manager for Commercial, Federal and/or Public pro...
Research Faculty (regardless of rank) - Persons with the titles of research assistant professor, research associate professor, or research professor. Assistant Professor - Physical Medicine and Rehabilitation Research Faculty. Tenure faculty (regardless of rank) - persons with the titles of professo...
In this role, you’ll be primarily responsible for the overall success of a variety of projects and will consult with clients and project teams to meet project deadlines from proposal to final invoice payment. Tasks supporting the management of construction materials testing projects, including daily...
Work with project stakeholders to gather detailed project requirements to ensure overall quality of delivery. Facilitate working session with project team members to develop detailed project schedules (Dates, Durations, Dependencies, & Owners). Work with project management team members to identi...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Senior Project Manager / Global Project Lead. ...
Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Shows pride upon project completion while providing exceptional customer service representing the Paul Davis brand. Confirms scope and budget before start of projects. Documents all phases of assigned projects· Ensures compliance with standards and regulations through consistent documentation. Sched...
Arcadis is seeking a Senior Bridge Project Manager to deliver projects in Ohio. In this position you will serve as a project manager and/or technical lead for infrastructure projects and direct the work of a multi-disciplinary team and junior engineering staff and CAD technicians. Serve as project m...
You will work closely with our data engineering team to ensure data integrity and availability, supporting various business intelligence and analytics initiatives. Assist in building and maintaining data pipelines using Python and SQL to ensure efficient data flow and integration across different sy...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
This job consults with cross-functional groups and levels to identify data and analytical needs, conduct analyses, review analyses and findings with leadership, facilitate related process/data improvement efforts, and develop executive level presentations. Develop and implement data collection syste...
Senior Project Manager to lead large-scale builds for multiple national repeat clients. Complex and exciting projects. Prepare and manage the project schedule . Complete monthly project status reports, owner billings and financial risk assessments. ...
The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requi...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
Prepares analysis to identify trends and issues, troubleshoot errors, validates data against other data sources, requirements and/or technical specifications, and work with data exchange processes and workflows between Company, government entities, and delegated entities to ensure accurate and compl...