Completion of a science-related Bachelor’s degree. Confirming adherence to all FDA, ICH-GCP and local regulations; Experience monitoring phase 1 trials.
Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. Evidence of a client focused approach.
College/University degree in Life Sciences or an equivalent combination of education, training & experience. Support regulatory team in preparing documents for…
Education *– A Bachelor’s degree, preferably in sciences. The role: *The Clinical Trial Assistant provides administrative support to all Project Managers in…
A Bachelor's degree in a health care or other scientific discipline or educational equivalent. Supporting the development of a subject recruitment plan.
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans,…
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…
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 or higher-level university degree in a medical- or mathematics-related field such as biology, epidemiology, pharmacology, health economics, or…
Support medical writing and clinical safety monitoring teams by performing quality control (QC) review of document deliverables, including clinical study…
Proactively manages mutually beneficial relationships with external partners relevant to the planning and implementation of clinical trials and improvement…
Participates in and may lead global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical…
Bachelor’s degree in health sciences or nursing (mandatory); Bachelor’s degree in health sciences or nursing (mandatory); 4 weeks’ vacation after one year.
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…
The Clinical Trial Associate 1 will assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by…
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…
Develop study safety data review plans and maintain a standard set of data review checklists for clinical trial laboratory data, AEs, serious AEs (SAEs),…
Support medical writing and safety monitoring teams by performing quality control (QC) review of document deliverables, including clinical study reports (CSR),…
BioLytical* is hiring an organized, flexible Clinical Research Associate to conduct virtual site visits, generate, prepare study protocols, ethics applications,…
Estimated: $56,440 -
$71,466 a year
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