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MomDoc
Clinical Research Coordinator
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Based on Arizona data
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$121,732 / year median in Arizona
+17% projected growth
Job Description
Clinical Research Coordinator MomDoc - 2.9 Scottsdale, AZ Job Details Part-time 2 hours ago Qualifications Informed consent English ECG equipment Collecting samples for laboratory testing Informed consent procedures implementation Patient care Data entry Patient recruitment Productivity software Blood pressure monitors Medical terminology Full Job Description Overview Women's health group seeks a Clinical Research Coordinator to care for patients in the Scottsdale area. Part-Time . Competitive pay. Great traditional and non-traditional benefits available, including six-week paid sabbaticals.
Must have strong computer skills in Microsoft Office applications.
Coordinating the operational aspects of new and ongoing clinical trials at the site.
Responsible for the execution of the protocol.
Patient recruitment and pre-screening.
Maintain and submit IRB communications and regulatory documents.
Timely communication with PI and lead study coordinator.
Ability to take and assess vitals ( i.e. blood pressure, pulse, height, weight).Qualifications1+ year Phlebotomy experience1+ year of EKG (ECG) experience1-2 years of Study Coordinator/Research Assistant1+ years of Patient RecruitmentCGP training and IATA training
While performing the duties of this job, the employee is occasionally required to walk and stand; frequently required to use hands; and regularly required to sit and talk or listen. May occasionally be required to lift up to 20 pounds.
SUMMARY A
Study Coordinator performs a variety of clinical study activities to assist the Investigator, Director, and Lead Study Coordinator in the conduct of a clinical study. this is a position with data entry, research, and medical assistant job duties.ESSENTIAL DUTIES AND RESPONSIBILITIES
include the following: (Other duties may be assigned as needed.)Must be proficient in medical terminology.Must have strong computer skills in Microsoft Office applications.
Coordinating the operational aspects of new and ongoing clinical trials at the site.
Responsible for the execution of the protocol.
Patient recruitment and pre-screening.
Maintain and submit IRB communications and regulatory documents.
Timely communication with PI and lead study coordinator.
Ability to take and assess vitals ( i.e. blood pressure, pulse, height, weight).Qualifications1+ year Phlebotomy experience1+ year of EKG (ECG) experience1-2 years of Study Coordinator/Research Assistant1+ years of Patient RecruitmentCGP training and IATA training
LANGUAGE ABILITY
Ability to read and interpret (in English) all documents, such as protocols, informed consents, and laboratory/procedure manuals. Ability to write (in English) routine reports and correspondence. Ability to speak effectively before groups of subjects, customers, or employees of WHR. Bilingual is a plus..PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.While performing the duties of this job, the employee is occasionally required to walk and stand; frequently required to use hands; and regularly required to sit and talk or listen. May occasionally be required to lift up to 20 pounds.