Providence, Rhode Island
SUMMARY: The Regulatory Coordinator performs multiple tasks in order to meet compliance requirements in research. This position will be overseeing clinical research regulatory requirements for the department. The Regulatory Coordinator will...
6d
| Job Type | Full Time |
Providence, Rhode Island
SUMMARY: Under general supervision of the Research Program Manager and the Director of the Center for Behavioral and Preventive Medicine (CBPM), and in accordance with established policies and procedures, the Research Project Director is re...
6d
| Job Type | Full Time |
Director, Clinical Quality Program Lead (Hybrid)
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General/Position Summary The Director, Clinical Quality Program Lead (CQPL) is responsible for the quality oversight across a range of study phases within assigned disease area(s) to ensure that trials are conducted in accor...
6d
| Job Type | Full Time |
Regulatory Coordinator - Radiological Sciences
Los Angeles, California
University of California - Los Angeles Health
Description This role is responsible for coordinating regulatory activities for clinical research studies across assigned units, departments, or divisions. The incumbent reviews clinical research protocols in detail and prepares, manages, a...
6d
| Job Type | Full Time |
Clinical Research Coordinator II - OBGYN
Milwaukee, Wisconsin
Purpose Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program's goals. Assist with recruiting, and training study staff. Primary Functi...
6d
| Job Type | Full Time |
Clinical Research Coordinator II - Medicine
Milwaukee, Wisconsin
Summary Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program's goals. Assist with recruiting, training, and supervising staff and mana...
6d
| Job Type | Full Time |
Research Regulatory Specialist - Wisconsin Institute of Neuroscience
Milwaukee, Wisconsin
Summary The Research Regulatory Specialist is responsible for gathering regulatory documents and preparing IRB applications, amendments, and continuing review submissions for human subject research, ensuring compliance with Federal, State, ...
6d
| Job Type | Full Time |
Associate Director for Clinical Trial Operations and Workforce Development
Milwaukee, Wisconsin
Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and Translational Science Institute (CTSI) at the Medical...
6d
| Job Type | Full Time |
Clinical Research Coordinator II - Neurology
Milwaukee, Wisconsin
Summary 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. Primary Responsibilities Recruit, screen, enroll and obtain ...
6d
| Job Type | Full Time |
Milwaukee, Wisconsin
Summary Manage all aspects of department clinical trial initiatives to ensure compliance with state, federal and institutional regulations, policies, and procedures. Primary Responsibilities Act as a resource for investigators and support s...
6d
| Job Type | Full Time |