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...
Build complex data sets from multiple data sources and write complex data flows using. Proficient in SQL, data models, data element dictionary and schema, with the ability perform data business analysis. Demonstrated knowledge of drug data file elements published by drug compendia/databases. Familia...
Build complex data sets from multiple data sources and write complex data flows using Databricks, SQL, Spark, and scripting languages (e. Proficient in SQL, data models, data element dictionary and schema, with the ability perform data business analysis. Demonstrated knowledge of drug data file elem...
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. ...
Build complex data sets from multiple data sources and write complex data flows using. Proficient in SQL, data models, data element dictionary and schema, with the ability perform data business analysis. Demonstrated knowledge of drug data file elements published by drug compendia/databases. Familia...
Are you an experienced Project Manager with a passion for construction and the agility to lead projects across various locations? Our client is seeking a Project Managers based in Ohio or open to full time travel, who specializes in Data Center construction, offering an opportunity to manage high-st...
We are seeking a highly skilled and motivated Project Manager with a strong background in transmission and substation projects. The ideal candidate will be responsible for leading and managing all phases of project execution, from initial planning and design through construction, commissioning, and ...
Works on multiple oncology trials.Quality of life focus wtih Regional Travel.Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team.Acts as Lead SM-training other SMs on study.Develops site start up ...
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...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
Clinical Trial Management professionals who can assist in this growth and contribute to the overall success of the organization. Oversee site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. ...
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 (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
As Data Integration Analyst JMETC, you will support test infrastructure test performance analysis and reporting, necessary to support expansion of joint distributed test events and effectively integrating live, virtual, and constructive (LVC) test resources. Tasks may vary from descriptions or stati...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Performs modeling of data sources and flows, works with data management staff to define an operational framework that will define, develop and implement policies and security frameworks to ensure precise and secure delivery of knowledge and information. Perform modeling of data sources and flows, wo...
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...
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. ...
Manages and executes daily on-site activities for multiple projects and leads project meetings with subcontractors, consultants, and stakeholders at frequent intervals to discuss problems, progress, and scheduling of work. Conducts frequent property inspections to ensure projects follow proper safet...
This is a fantastic opportunity for a Operational Readiness Project Manager to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn. Operational Readiness Project Manager - Ohio, US...
This is a fantastic opportunity for a CAPEX Project Manager to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn. CAPEX Project Manager– 12 month Contract – Ohio. Assist the Glob...
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. ...