The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Strong understanding of medical and clinical research term...
Looking for someone who might have a background in phlebotomy or specimen processing, Preferred but not required Summary:The main function of a clinical trials assistant is to assist the clinical research teams in ensuring the most effective and efficient conduct by providing administration and proj...
Role Summary: The Clinical Research Coordinator is responsible for managing in-house clinical research for the Clients Ultrasound Businesses. Previous experience with a minimum of 2 years in clinical research. Previous experience as a Clinical Research Coordinator. Coordinate and oversee research se...
The Clinical Research Coordinator is responsible for managing in-house clinical research for the Client Ultrasound Businesses. Title – Clinical Research Coordinator. Previous experience with a minimum of years in clinical research. Previous experience as a Clinical Research Coordinator. ...
Looking for someone who might have a background in phlebotomy or specimen processing, Preferred but not required Summary:The main function of a clinical trials assistant is to assist the clinical research teams in ensuring the most effective and efficient conduct by providing administration and proj...
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...
Talascend is seeking a professional, skilled individual for our Clinical Research Associate position located in Wauwatosa, WI. Previous experience with a minimum of 2 years in clinical research. Previous experience as a Clinical Research Coordinator. Coordinate and oversee research sessions, includi...
The Clinical Research Coordinator is responsible for managing in-house clinical research for the Client Ultrasound Businesses. Title – Clinical Research Coordinator. Previous experience with a minimum of 2 years in clinical research. Previous experience as a Clinical Research Coordinator. ...
Looking for someone who might have a background in phlebotomy or specimen processing, Preferred but not required Summary:The main function of a clinical trials assistant is to assist the clinical research teams in ensuring the most effective and efficient conduct by providing administration and proj...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
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. ...
Role Summary/Purpose The Clinical Research Coordinator is responsible for managing in-house clinical research for the HC Ultrasound Businesses. Title – Clinical Research Coordinator. Posted Position Title Clinical Research Coordinator. Previous experience with a minimum of years in clinical research...
The Clinical Research Coordinator is responsible for managing in-house clinical research for the Client Ultrasound Businesses. Title – Clinical Research Coordinator. Previous experience with a minimum of 2 years in clinical research. Previous experience as a Clinical Research Coordinator. ...
The Project Manager - Internal will play a critical role in managing and executing corporate projects, with a particular focus on research and development (R&D), enterprise resource planning (ERP) implementation and improvements, and smaller departmental projects. Facilitate regular project meetings...
Coordinate the day-to-day administrative activities of a health-disparities/health equity focused clinical research and health improvement program. ...
Perform the day-to-day administrative activities of clinical research trial programs. Minimum Required Experience: 2 years clinical research coordination. Preferred Experience: Previous oncology clinical research coordination. Field: ...
Perform the day-to-day administrative activities of the department's clinical research program, primarily supporting research in the Division of Minimally Invasive and Gastrointestinal Surgery (MIGS). Coordinate research protocols including arranging necessary appointments and procedures, working co...
Perform the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program's goals and offer research opportunities to pediatric patients with a range of endocrine and growth disorders, including thyroid conditio...
Collect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized database. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and main...
Clinical Research Coordinator III/Regulatory Specialist-IRB. Clinical Research Coordinator III. Work closely with Research Managers and Research Coordinators to identify and complete all regulatory needs associated with each assigned protocol. Coordinate the day-to-day administrative activities of t...
Clinical Research Coordinator I - GOOD Study. ...
The Statistical Research Scientist will be involved in every aspect of the research enterprise, including study design and consultation with basic scientists and clinicians, data management, analysis, and preparation of progress report and manuscripts. The Statistical Research Scientist will support...
Research Program Coordinator I. Department of Medicine's Center for International Blood and Marrow Transplant Research. CIBMTR) you will work independently under the administrative direction of the Program Director to coordinate the day-to-day program activities of the Observational Research Program...
Graduation from an accredited Medical Assistant training program or a Licensed Practical Nurse (LPN) license. Medical Assistant experience in is preferred. Medical Assistant certificate of completion from an accredited program or LPN license. ...
As a Project Coordinator in our Lake Services Division, you are responsible for the scheduling/coordination of projects, day to day activities, client relations, and lakes staff workload on your projects, as well as assisting on lakes projects managed by other staff. Lakes Division Project Coordinat...