Part-Time Clinical Research CoordinatorThis is a contract role and requires previous clinical research experienceJob Description:Looking to hire an onsite part time individual with clinical research experience to act as a consultant CRC to support an ongoing clinical trial. Responsibilities:Chart re...
Clinical Research Program Coordinator will maintain knowledge of study protocols and assist in the daily operations of the recruitment under the direction of the Principal Investigator and Co-Investigators and will manage and coordinate patient related tasks of Cardiology/Electrophysiology patients ...
Maintain Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA). Clinical Research Coordinator III (RN). The Alaka`ina Foundation Family of Companies is looking for a qualified Clinical Research Coor...
Clinical Research Program Coordinator will maintain knowledge of study protocols and assist in the daily operations of the recruitment under the direction of the Principal Investigator and Co-Investigators and will manage and coordinate patient related tasks of Cardiology/Electrophysiology patients ...
Performs a variety of complex duties to support the conduct of clinical research, such as, facilitating the informed consent process, coordinating required research activities; collecting, compiling, and documenting clinical research data to ensure adherence to protocols and validation of informatio...
ERP International, LLC () is currently seeking a Clinical Research Coordinator II for a full-time position supporting the Walter Reed Army Institute of Research (WRAIR) at Silver Spring, MD. ...
Performing routine and for-cause monitoring of human subjects research and protocols that received research determinations to ensure the appropriate regulations were applied during the review of the study and ensuring the research/activity is conducted as approved. Knowledge and experience in the ar...
Sparks Group, partnered with a leading healthcare research institute, has an immediate need for a detail-oriented Clinical Trials Revenue Cycle Coordinator II. This coordinator will play a critical role in ensuring accurate and compliant billing for clinical trials, collaborating with revenue cycle ...
Maintain Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA). Organize and prioritize all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a...
Providing clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data. We are looking for experi...
Concentric Methods is seeking a Clinical Research Coordinator to join our team in Bethesda, MD, in support of the NIH. Supports clinical staff develop, implement, and maintain clinical research data files and materials. Assist staff writing and editing clinical research protocols and informed consen...
RESPONSIBILITIES Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data; Attend all...
Clinical Research Coordinator II. The Clinical Research Coordinator II will primarily support the HIV Natural History Study. HJF's support and administrative capabilities allow military medical researchers and clinicians to maintain their scientific focus and accomplish their research goals. This po...
ERP International, LLC () is currently seeking a Clinical Research Coordinator I for a full-time position supporting the Walter Reed Army Institute of Research (WRAIR) at Silver Spring, MD. ...
As a member of the Protocol Operations team, develop clinical research protocols and informed consents for evaluation of investigational vaccines and monoclonal antibodies, including but not limited to the following tasks: conduct background research on infectious diseases targets and any already de...
As a member of the Protocol Operations team, develop clinical research protocols and informed consents for evaluation of investigational vaccines and monoclonal antibodies, including but not limited to the following tasks: conduct background research on infectious diseases targets and any already de...
Works closely with Revenue Cycle teams to resolve clinical research billing errors. Facilitate audit of ongoing clinical trials for accuracy and compliance with applicable. Ensure timely and accurate clinical trial invoicing as assigned. Invoice all active clinical trials consistent with contract te...
Education & Training: Associate’s degree in related field and Certified Clinical Research Professional (CCRP) or another research specific certification is strongly preferred. Work Orientation & Experience: At least three (3) years’ experience in clinical research with at least one (1) year ...
The NIAID Transition Program in Clinical Research provides an exceptional opportunity for physicians to gain clinical and translational research experience in the NIAID Division of Intramural Research (DIR). The NIAID Transition Program in Clinical Research seeks up to three candidates for three- to...
The primary focus of this position is to serve as the Project Manager/Lead on the engineering development and design of bridge projects within the Bridge/Structures Design Division. Project Manager - Bridges/Structures. Actively manage and oversee the work of Project / Design Engineers and Engineeri...
Lead legal team members supporting the successful development and implementation of products, programs, and projects. Project Management Institute, Inc. JobPosting","title":"Manager, Global Compliance","datePosted":"2024-08-26T00:00:00","validThrough":null,"description":"What you will be doing\nYou ...
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into pub...
We are currently seeking a Program Manager - Cloud Support Services to join our team in Bethesda, Maryland (US-MD), United States (US). NTT DATA is seeking a highly motivated and experienced Program Manager to lead the successful delivery of Cloud Support Services for a federal scientific research a...
The Senior Clinical Research Associate (CRA) is responsible for monitoring clinical study sites either on-site at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all ap...
FJpe-cbaA7g?si=ula_iBAkPPb7PTPm (Copy and paste into browser) Reporting to the Clinical Programs Manager, the Clinical Coordinator is responsible for working collaboratively with the patient care team to promote the safe and effective use of medications. The Clinical Coordinator also takes a leading...