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...
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. ...
Data Quality Assurance: Implement and monitor data validation processes to ensure the integrity of the data used in analysis, including identifying and correcting inconsistencies and errors. SQL: Strong proficiency in SQL to query databases, manipulate large datasets, and perform complex data joins ...
The Data Analyst will: aggregate and perform advanced statistical analysis on business data; Integrate data from multiple data sources or functional areas, ensure data accuracy and integrity; Write advanced queries or reports to provide data for various analytical projects; Identify, analyze, and in...
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...
Provide project manager leadership and help foster a work culture that recognizes, supports individual differences in work-styles, personalities, cultures and values to maximize team performance and effectively achieve project goals and timelines. Responsible for providing project planning for estab...
This individual will be a member of the local quality team that supports preclinical and clinical gene therapy research functions. The candidate will have a clear understanding of the data capture process and will perform QC review of gene therapy research data under direct supervision. ...
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. ...
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. Associate Director, Project Management. ...
Gastro Health is seeking a Full-Time Research Assistant to join our team!. Any other task assigned by the Clinical Research Coordinators and Central Hub Protocol Preparation & Review Attends investigator meetings as required or requested by the PI and Clinical Research Coordinator. Maintains ef...
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...
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...
At least 5 years experience in civil engineering site plan design consulting.Professional license registration in the state of Ohio.Strong electronic design skills (preferably Civil 3D).Civil engineering design skills with a focus on site planning, grading, utility systems, stormwater management, sa...
Why not take your career to new heights as a Data Quality Analyst and contribute meaningfully to our journey of innovation and business expansion? In this role, you'll play a pivotal part in driving business transformation through data-driven solutions, thus becoming a catalyst for progress and succ...
Client management, including responding to RFP’s for research, developing study budgets and amendments. Executes and contributes to the design of research studies in concert with our clients and/or business partners. Requires a MS, MPH, PharmD, PhD, or MD in business or a life sciences field and at ...
As a CRA 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 instructions to site personnel and...
Have a strong understanding and application of project management principles, concepts, practices, and standards to coordinate and manage broad analysis projects. R&D data collection and management, project-level and program-level. Master’s or Doctoral degree with 6+ years of analysis project manage...
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...
The incumbent delivers data profiling, conducts testing and systems validation to troubleshoot data anomalies, monitors data management metrics and data loads. This job understands healthcare data from end-to-end and analyzes raw data and analytic data for the enterprise. Verify analytic data for th...
We are looking for a Scientist- Experienced Products Research / Product Development to join the 1TPT Organization. This is an upstream R&D role where developing products research mastery, leadership and multi-functional collaboration will be essential for your day to day work. Consumer Market Resear...
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. ...
Data Analysis Reporting experience. Experience as Business Analyst preferred. ...