Hiring.Camp

Clinical Research Coordinator - PRN

Ccf

·

Yesterday

Location
Cleveland Clinic Main Campus, United States of America · Remote Location
Workplace
Remote
Type
Part-time
Department
Healthcare
Education
Bachelor
Closing date
Today
Source
Workday

Description

                    

At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day.

                        

We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One.

                                    

Job Title

Clinical Research Coordinator - PRN

                        

Location

Cleveland

                    

Facility

Cleveland Clinic Main Campus

                     

Department

Cancer Center Research-Cancer Institute

                      

Job Code

D99967

                     

Shift

Days

                       

Schedule

8:00am-4:30am

                       

Job Summary

Coordinates the compliant implementation and conduct of human subject research projects typically of low workload and low complexity.

                         

Job Details

Responsibilities:

  • Assists with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements which may include:  maintenance of regulatory documents and binders, data management, IRB submissions and communication of such to the research team. 
  • May be responsible for reporting/completion of Serious Adverse Events and/or safety log as defined per protocol as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines as applicable. 
  • Communicates with sponsors, monitors, research personnel to ensure all aspects of study compliance.
  • Collaborates with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits. 
  • May collaborate with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment. 
  • Monitors and reports project status. 
  • Completes regulatory documents, data capture and monitoring plans.
  • Assists with completion of protocol related activities. 
  • As delegated, may be required to attain and maintain clinical competencies for unlicensed caregivers such as phlebotomy, vital signs, ECG, POC testing and other testing as required.  
  • Monitors research data to maintain quality.
  • Understands basic concepts of study design. 
  • Demonstrates comprehension of assigned research protocols. 
  • Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. 
  • Assists with preparation for audits and response to audits.
  • May assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures.
  • Maintains study personnel certification records (License, CV, CITI).
  • Maintains professional relationships, including frequent and open effective communication with internal and external customers.
  • Documents the education and training of research personnel as needed. 
  • May participate in the conduct and documentation of the informed consent process.
  • May contribute to research project budget development.
  • Performs other duties as assigned.

Education:

  • High School Diploma or GED.  Associate or bachelor's degree in health care or science related field preferred.  Degree may offset experience requirement.

Languages:

  • Language required.
  • Language preferred

Certifications:

  • None required.

Complexity of Work:

  • Requires excellent organizational, written, and verbal communication skills.
  • Must be able to take direction and appropriate action in a stressful environment.
  • Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing spreadsheets, database and presentation software, and the ability to undertake internet searches.
  • Solid written and verbal communication skills.
  • Must be self-directed with demonstrated ability to work in collaboration and cooperation with members of a multidisciplinary team.
  • Within 90 days of hire, must successfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic.

Work Experience:

  • Minimum two years clinical research or healthcare experience required.
  • Associate or bachelor's degree in healthcare or science field may offset experience requirement.
  • Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing, spreadsheets, database and presentation software, and the ability to undertake internet searches. Solid written and verbal communication skills.

Physical Requirements:

  • Ability to perform work in a stationary position for extended periods
  • Ability to operate a computer and other office equipment
  • Ability to communicate and exchange accurate information
  • In some locations, ability to move up to 25 pounds

Personal Protective Equipment:

  • Follows standard precautions using personal protective equipment as required.

                       

The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances.

Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption.

Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. 

If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/

Please review the Equal Employment Opportunity poster

                  

Cleveland Clinic is pleased to be an equal employment opportunity employer.

Skills

GCPFDACompliance

Similar Jobs

30

Clinical Research Coordinator

CenExel·Englewood, CO

Today

Clinical Research Coordinator

Saintlukes·Saint Luke's Hospital, MO

1d ago

Clinical Research Coordinator

Providence Health & Services·Fullerton, CA·Onsite

1d ago

Clinical Research Coordinator

CARE Fertility·Bedford, TX

1d ago

Clinical Research Coordinator

Alcanza Clinical Research·Phoenix Medical Trials - Gilbert, AZ

2d ago

Clinical Research Coordinator

Grider Support Services·Buffalo, NY

4d ago

Clinical Research Coordinator

Thermofisher·US - Richfield, MN - 6601 Lyndale Avenue South·Onsite

5d ago

Clinical Research Coordinator

Massgeneralbrigham·221 Longwood Avenue Boston, US·Hybrid

5d ago

Clinical Research Coordinator

Mayo Clinic·Phoenix, AZ

5d ago

Clinical Research Coordinator

Providence Health & Services·Spokane, WA·Onsite

6d ago

Clinical Research Coordinator

The Remedy·Vadnais Heights, Minnesota

6d ago

Clinical Research Coordinator

Alcanza Clinical Research·Coastal Carolina Research Center, SC

6d ago

Clinical Research Coordinator

Oneoncology·Fountain Valley, CA

1w ago

Clinical Research Coordinator

Affiliates Commonspirit·PHOENIX, AZ

1w ago

Clinical Research Coordinator

Franciscanalliance·IN - Indianapolis, US

1w ago

Clinical Research Coordinator

Genesiscare·NSW-St Leonards-North Shore Health Hub, Australia

1w ago

Clinical Research Coordinator

Massgeneralbrigham·221 Longwood Avenue Boston, US·Onsite

1w ago

Clinical Research Coordinator

Massgeneralbrigham·55 Fruit Street Boston, US·Onsite

1w ago

Clinical Research Coordinator

Advanced Urology Institute·North Charleston, SC

1w ago

Clinical Research Coordinator

Tandem Intermediate LLC·Freehold, NJ

1w ago

Clinical Research Coordinator

Thermofisher·US - Birmingham, AL - 832 Princeton Avenue SW·Onsite

1w ago

Clinical Research Coordinator

New York Cancer and Blood Specialist·Research - Lake Success 1, NY

1w ago

Clinical Research Coordinator

Genevausa·Fort Jackson, US·Onsite

1w ago

Clinical Research Coordinator

Wisconsin·Medical Sciences Center-0450, US·Onsite

1w ago

Clinical Research Coordinator

Massgeneralbrigham·15 New Chardon Street Boston, US·Hybrid

1w ago

Clinical Research Coordinator

Sarasota Arthritis Center·Sarasota, FL·Onsite

1w ago

Clinical Research Coordinator

Springfield Clinic·Springfield, IL·Onsite

1w ago

Clinical Research coordinator

Advocate Health·Rome, GA - 1825 Martha Berry Blvd NE

2w ago

Clinical Research Coordinator

Careers With Purpose·Sanford Broadway Med Bld, US

2w ago

Clinical Research Coordinator

Massgeneralbrigham·125 Nashua Street Boston, US·Onsite

2w ago