Meditrial is looking for a certified and experienced clinical research associate (CRA) experienced in medical device clinical trial monitoring, EDC systems,…
Bachelor’s degree in a health or scientific related program. Experience performing clinical assessments, including but not limited to obtaining vital signs,…
Clinical research coordinators will be working under the direction of the Principal Investigator, responsible for supporting the successful conduct of clinical…
Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. Evidence of a client focused approach.
Completion of a science-related Bachelor’s degree. Confirming adherence to all FDA, ICH-GCP and local regulations; Experience monitoring phase 1 trials.
Aider les Gestionnaires et les Associés à la Recherche Clinique (ARC) à mettre à jour et à maintenir avec précision les documents cliniques et les systèmes (p…
Under the supervision of the Heart-in-a-Dish Manager, the employee’s goal is to assist the team with medical chart review, data entry, data mining and compiling…
Exercising poor judgment and lack of appropriate consultation with other team members can adversely affect the productivity of the research program and might…
The CLINICAL RESEARCH COORDINATOR plans, implements and coordinates all aspects of study visits according to study protocol; obtains informed consent, takes…
Pharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trails in healthy volunteers, special and…
We provide peer-friendly education about disease, state-of-the-art antiviral medications and comprehensive support during and after treatment within an open,…
Advises investigators on Canadian federal and provincial regulatory requirements and TCPS2 2014 requirements for conducting human research as well as specific…
May participate in the study development and start-up process including reviewing protocols, drafting of the Monitoring Plan, designing and/or reviewing CRFs,…
O Assist in design, implementation and coordination of all aspects of data collection, source documentation and CRF transcription as per protocol, SOPs and ICH…
A university degree in health or social sciences, public health or a related discipline; As well as at times may assist with implementation projects focused on…
As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive…
Provides guidance and support to investigators, clinical research coordinators, research nurses, pharmacists, data entry clerks, CCTG personnel as required.
The individual will work closely with the Principal Investigators, study team and stakeholders to coordinate the multiple clinical research studies in the…
Bachelor’s degree in a health or scientific related program. Our Medical Director, Dr. Sharon Cohen, a Canadian-trained behavioural neurologist, along with her…
This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor's satisfaction, and that studies are run according to…
Create Job Alert
Provide an Email Address
You will receive email alerts about new jobs matching your search.
