Skip navigation
Unable to save this job. Please try again later.

{msg}

Email this Job to Yourself or a Friend

To begin the application process, please enter your email address.

Company Contact Info

  • Kokomo, IN

Already have an account?

Sign in to apply with your saved resumes.

New to CareerBuilder?

Don't have an account? Continue as a guest!

Sorry, we cannot save or unsave this job right now.

Report this Job

Trust and Site Security Team.

Don't miss out on new jobs!

Get the latest Clinical Research Coordinator (Management) jobs in Kokomo, IN delivered directly to your inbox. You can unsubscribe at any time.

Saving Your Job Alert

Job Alert Saved!

Could not save Job Alert!

You have too many Job Alerts!

This email address has reached the maximum of 5 email alerts. To create a new alert, you will need to log into your email and unsubscribe from at least one.

Sign Up

or   Sign In Here
Password Must Contain
• 
8 to 15 characters
• 
1 uppercase letter
• 
1 number or symbol
• 
1 lowercase letter
Cancel
Create an Account with CareerBuilder to save jobs & unlock these great features
See similar job titles and skills to help you make your next move
Upload a resume and become visible to Hiring Managers and Employers
Compare Salary Information to see where you stand amongst your peers
Easily Quick Apply to jobs with just one click!

Email Send Failed!

Clinical Research Patient Specialist Campus Kokomo

Indiana University • Kokomo, IN

Posted 1 month ago

Job Snapshot

Full-Time
Experience - 2 years
Degree - 4 Year Degree
Education - Teaching - Administration
Research

Job Description

The IU Simon Cancer Center’s Clinical Trials Office (IUSCC CTO) is currently seeking a multi-disciplinary Clinical Research Patient Specialist (CRPS). The CRPS will coordinate both sponsor initiated and investigator initiated oncology focused clinical trials.

The CRPS will screen and identify potential study participants from a review of protected health information based on protocol eligibility criteria, and will consent study participants which includes a discussion of procedures and tests. The CRPS will also ensure the Informed Consent documents are properly signed prior to the start of the study; and will identify and schedule screening procedures to confirm study participant eligibility and enrollment on clinical trials. Additionally, the CRPS will collaborate with insurance coordinators, clinical coordinators and/or research nurses to obtain insurance verification for standard of care procedures. This position will also schedule and coordinate research related services such as infusions, radiology and other research related services.


Job Requirements

REQUIRED: Bachelor’s degree in Science or a health-related field and two years of experience in clinical research; OR Bachelor’s degree in other disciplines or Associate’s Degree in Allied Health professions and three years of experience in clinical research. Clinical Research Certification (ACRP or SOCRA).

Ability to effectively communicate and exchange information, organizational skills, and the ability to develop and maintain a rapport with professional, study participants and families. Knowledge and understanding of case report forms, research documentation, research methods and study protocols. Ability to read, understand and communicate complex scientific and clinical information. Ability to work as a team player maintain and manage conflicts and resolve problems effectively. Ability to attend regular scheduled meetings (weekly, monthly and team). High degree of accurate and organized records and work with some level of independence. Strong interpersonal skills and extensive judgment to appropriately respond to participants, family and research staff. Proficient use of computers, strong attention to detail and the ability to multi-task are also necessary.


Preferred Qualifications 
Working Conditions / Physical Demands 

Working in a fast-paced environment (Clinics) and may be sitting or standing for long periods of time.


Salary Range 
Job ID: 11511P
Help us improve CareerBuilder by providing feedback about this job: Report this Job.
CAREERBUILDER TIP
For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.
By applying to a job using CareerBuilder you are agreeing to comply with and be subject to the CareerBuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.
Don't miss out on new jobs like this
Get the latest jobs delivered to your inbox. Unsubscribe at any time.

Saving Your Job Alert

Job Alert Created

Well, this is embarrassing. We are having trouble saving your search. You can try again or come back at a later time.

Maximum Email Alerts

This email address has reached the maximum of 5 email alerts. To create a new alert, you will need to log into your email and unsubscribe from at least one.