Monster.ca

Clinical Research Associate

Clinical Research Manager

Clinical Trial Manager

Clinical Research Director

Clinical Project Manager

A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control. 

Clinical Research Coordinator

A source document is a document in which data collected for a clinical trial is first recorded. This data is usually later entered in the case report form. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH-GCP) guidelines define source documents as "original documents, data, and records." Source documents contain source data, which is defined as "all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial."

Source Document

Informed consent is a principle in medical ethics and medical law that a patient should have sufficient information before making their own free decisions about their medical care. A healthcare provider is often held to have a responsibility to ensure that the consent that a patient gives is informed, and informed consent can apply to a health care intervention on a person, conducting some form of research on a person, or for disclosing a person's information. Informed consent is, in fact, a fundamental principle in the field of health protection, obviously wanting to mark the very close and unavoidable connection between the need for consent and the inviolability of the right to health. A health care provider may ask a patient to consent to receive therapy before providing it, a clinical researcher may ask a research participant before enrolling that person into a clinical trial, and a researcher may ask a research participant before starting some form of controlled experiment. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics.

Informed Consent

Clinical Research Coordination

CRFS  is a network file system protocol by Zach Brown formerly of Oracle intended to leverage the Btrfs architecture to gain higher performance than existing protocols and to expose Btrfs features such as snapshots to remote clients. The code is unmaintained.

Coherent Remote File System (CRFS)

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	Median Salary
Goodwood, Ontario	$71,936
National	$68,864
Location +/-	4% Higher
	Search another salary
	Show me related jobs

Location	Median Salary
Goodwood, Ontario	$71,936
National	$68,864
Location +/-	4% Higher
	Search another salary
	Show me related jobs

Salary Estimate for Goodwood, Ontario
Nearby Locations...

Salary Details

Boost Your Value

Boost Your Value

Advance your career

Advance your career

Jobs In on Monster

Clinical Research Coordinator Salary Estimate for Goodwood, OntarioNearby Locations...

Salary Details

Boost Your Value

Boost Your Value

Salary for Related Jobs

Salary for Related Jobs

Advance your career

Advance your career

Jobs In on Monster

Salary Estimate for Goodwood, Ontario
Nearby Locations...