The intuitive web page software for Clinical trial managers

Summary of Responsibilities: Manage and lead cross-functional study teams, including vendors; liaise with other functional areas (preclinical development, pharmaceutical sciences, safety, and regulatory affairs) in order to accurately coordinate clinical study activities.

ClinicalTrials.gov is a registry and results database of privately and publicly funded clinical studies conducted around the world. The resource is provided by the U.S. National Library of Medicine. Each study record includes a summary of the study protocol.

Factors such as patient population, site experience in clinical research, trial phase requirements, patient safety, ethical oversight, and cost-effectiveness must be carefully considered during site selection.

Clinicaltrials.gov is the largest clinical trials registry. Clinical trials conducted in the United States are required to be registered in the registry.

Working with data, establishing what to evaluate and how to measure it as well as recording the data. Avoiding bias, preventing situations such as assigning certain patients to certain groups based on a desired outcome. Maintaining safety standards, protecting those involved in the trial.

Those who enjoy organising and managing projects from a top-down approach would likely be better suited to a role as a Clinical Project Manager. For those who prefer to focus and get hands-on with clinical trials and managing other team members, a role as a Clinical Trials Manager may be a better option for you.

To start your search: Go to .clinicaltrials.gov. Click on the link, Search for Clinical Trials, on the home page. Enter your search terms -- for example, a disease or intervention and a location: heart attack AND aspirin AND California. Separate your multiple search terms with a capitalized AND.

ClinicalTrials.gov gives you information about a trials purpose, who may participate, locations, and phone numbers for more details. This information should be used in conjunction with advice from health care professionals.

Responsible for managing site investigator relationships and executing site start up and performance plans, assigning tasks and deadlines to site clinical teams, directing and monitoring clinical site work efforts on a daily basis, identifying resource needs, performing quality reviews, and escalate functional, quality

Typically, clinical trial managers have a masters or graduate certificate, although some can begin working with just a bachelors. Clinical trial work experience is critical; however, a professional must understand how trials run before they ever step into managing one.