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A Clinical Research Director is responsible for the overall research strategy of an organization undertaking clinical trials, usually pharmacological drug testing.

Directeur de la recherche et du développement

Responsable/directeur de biostatistique

Responsable des affaires réglementaires

Directeur de la sécurité des patients

Directeur de communication mondiale

Directeur de recherche clinique


The Common Technical Document (CTD) is a set of specifications for an application dossier for the registration of Medicines and designed to be used across Europe, Japan and the United States. It is an internationally agreed format for the preparation of applications regarding new drugs intended to be submitted to regional regulatory authorities in participating countries. It was developed by the European Medicines Agency, the Food and Drug Administration and the Ministry of Health, Labour and Welfare (Japan). The CTD is maintained by the International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

Common Technical Document

Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical research is different from clinical practice. In clinical practice established treatments are used, while in clinical research evidence is collected to establish a treatment.

Clinical Research

Clinical trials are experiments or observations done in clinical research. Such prospective biomedical or behavioral research studies on human participants are designed to answer specific questions about biomedical or behavioral interventions, including new treatments and known interventions that warrant further study and comparison. Clinical trials generate data on safety and efficacy. They are conducted only after they have received health authority/ethics committee approval in the country where approval of the therapy is sought. These authorities are responsible for vetting the risk/benefit ratio of the trial—their approval does not mean the therapy is 'safe' or effective, only that the trial may be conducted.

Clinical Trials

Good clinical practice (GCP) is an international quality standard, which governments can then transpose into regulations for clinical trials involving human subjects. GCP follows the International Council on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), and enforces tight guidelines on ethical aspects of clinical research.

Location	Salaire médian
Calgary, AB	$84,240
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Location	Salaire médian
Calgary, AB	$84,240
National	$84,240
Emplacement +/-	0% Supérieur
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	Montrez-moi les emplois associés

Directeur de recherche clinique Estimation salariale pour Calgary, AB
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Directeur de recherche clinique Estimation salariale pour Calgary, AB
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