Meditrial is looking for a certified and experienced clinical research associate (CRA) experienced in medical device clinical trial monitoring, EDC systems,…
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.
May participate in the study development and start-up process including reviewing protocols, drafting of the Monitoring Plan, designing and/or reviewing CRFs,…
College/University degree in Life Sciences or an equivalent combination of education, training & experience. Support regulatory team in preparing documents for…
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
Familiarity with HPLC/UPLC, fluorescence/absorbance spectroscopy, general laboratory/analytical techniques, statistical design of experiments, data modeling,…
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…
Valid driver’s license and passport are required. Interact with internal groups including data management, pharmacovigilance, quality assurance and business…
A Bachelor's degree in a health care or other scientific discipline or educational equivalent. Supporting the development of a subject recruitment plan.
Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical…
Plan and perform the realist evaluation: Collect qualitative data: interviews and focus groups with patients after they received CBT, as well as with the…
Bachelor’s degree in life sciences. Development of clinical project plan including the monitoring plan. Preparation of clinical trial documentation including…
Master's degree in a relevant field and 2 years of related experience or a Bachelor’s degree with 5 years of related. Help with the execution of the study.
Bachelor’s degree in health sciences or nursing (mandatory); Bachelor’s degree in health sciences or nursing (mandatory); 4 weeks’ vacation after one year.
Support medical writing and clinical safety monitoring teams by performing quality control (QC) review of document deliverables, including clinical study…
Education *– A Bachelor’s degree, preferably in sciences. The role: *The Clinical Trial Assistant provides administrative support to all Project Managers in…
The individual will work closely with and assist Dr. Vigod and study team members in research and program administrative tasks, specifically on a Health Canada…
Develop study safety data review plans and maintain a standard set of data review checklists for clinical trial laboratory data, AEs, serious AEs (SAEs),…
Proactively manages mutually beneficial relationships with external partners relevant to the planning and implementation of clinical trials and improvement…
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…
L'Institut Lady Davis* est à la recherche d'un professionnel expérimenté pour remplir le rôle clé d' *associé de recherche clinique *dans notre département de …
$55,000 -
$60,000 a year
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