The growing team at the CTU is comprised of a Director of Clinical Trials Operations, Clinical Site Manager, Clinical Trial Associate, and Licensed Clinical Nurses with strong experience in clinical trials. Active private practice with patients available for clinical research or access to patients w...
The Clinical Research Nurse will provide clinical support in the Cardiovascular Research clinical trials office. The Clinical Research Nurse role is the specialized practice of professional nursing focused on maintaining equilibrium between care of t Clinical, Research, Nurse, Healthcare, Staffing, ...
We are seeking a Clinical Research Coordinator to join our team and contribute to a NIH-funded study on acute respiratory distress syndrome (ARDS) recovery. Conduct outpatient clinic research follow-up visits, including repeating questionnaires, measures of physical function, and phlebotomy. ...
The Clinical Research Assistan. As a partner with the Certified Medical Assistants, the position will also work as a MA while not performing clinical research duties. High School diploma; prefer an associate degree for clinical research work. ...
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...
As a Clinical Research Associate 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 instructio...
Profound enables community physicians to offer clinical research as a therapeutic option to their patients. Work with the clinical research coordinator in providing in-service education on new protocols to study and clinic/hospital staff as needed. Assess study-specific procedures along with the cli...
The Clinical Research Coordinator will support multiple research studies (government, private and pharmaceutical) through the coordination and implementation of clinical trials and protocols involving human subjects. Responsible for screening, enrollment, and treatment of research subjects in compli...
Clinical Research Coordinator I The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...
Under the supervision of the investigator(s) and research coordinator, and following established policies and procedures, performs a variety of clinical research activities, and participates in carrying out research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. ...
Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Department: Cancer Clinical & Trans Resear. Our superior care and discoveries ...
Profound Research: Profound Research, a Rubicon Founders portfolio company, seeks to drive clinical innovation through clinical research. Profound Research is looking to build an energetic team inspired by changing how patients and providers engage in clinical research. Profound enables community ph...
POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data. The position will work with principal investigators and other research team members to accurately and efficiently carry out a ran...
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. ...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
As a Clinical Research Associate 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 instructio...
Field Clinical Research Specialist. Assist with preparation of/revisions to the Clinical Investigation Plan for assigned clinical studies. Interface with representatives from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clini...
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. ...
Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Department: Cancer Clinical & Trans Resear. Our superior care and discoveries ...
The Clinical Research Coordinator will support multiple research studies (government, private and pharmaceutical) through the coordination and implementation of clinical trials and protocols involving human subjects. Facilitate screening, enrollment, and treatment of research subjects in compliance ...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
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...
We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials. Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level posit...
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...