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Clinical Research Coordinator II – RI Translational Bird

  • Permanent
  • Anywhere

Website Nationwide Children's Hospital

Nationwide Children's Hospital

Company : Nationwide Children’s Hospital

Country: United States

Location : Columbus, Ohio

Post: Thu, 09 Sep 2021 00:58:50 GMT

Expires: Thu, 07 Oct 2021 23:59:59 GMT

Apply Job : Apply Online

—————————— Job Description ——————————

Overview:
Clinical Research Coordinator II – RI Translational Bird

 

The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a study and study closure activities. The CRC II also trains and mentors other CRC’s to ensure consistency in study management activities.

 

Schedule: (Full time, Benefits Eligible)

 

Location:

Wexner Center700 Children’s DrColumbus, Ohio 43205

Why Nationwide Children’s Hospital?:
The moment you walk through our doors, you can feel it. When you meet one of our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it, too. Welcome to Nationwide Children’s Hospital, where Passion Meets Purpose.

Here, Everyone Matters. We’re 13,000 strong. And it takes every single one of us to improve the lives of the kids we care for, and the kids from around the world we’ll never even meet. Kids who are living healthier, fuller lives because of the knowledge we share. We know it takes a Collaborative Culture to deliver on our promise to provide the very best, innovative care and to foster new discoveries, made possible by the most groundbreaking research. Anywhere.

Ask anyone with a Nationwide Children’s badge what they do for a living. They’ll tell you it’s More Than a Job. It’s a calling. It’s a chance to use and grow your talent to make an impact that truly matters. Because here, we exist simply to help children everywhere.

Nationwide Children’s Hospital. A Place to Be Proud

Responsibilities:
Conducts clinical studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout study; adheres to good clinical practices.

Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects rights through institutional IRB, federal and state regulations; Ensures the subject meets inclusion/exclusion criteria; answers questions related to the protocol procedure as applicable; acts as a patient/family advocate;

Coordinates, and schedules subject study visits with other hospital services and the PI/sub-I; manages protocol required data; performs study procedures according to recognized skill level and certifications and within the local and federal regulations and guidelines; collects, processes and ships human specimens for use in research studies

Identifies study implementation and/or study management issues and works with the study team to develop and implement solutions to ensure study progress and success

Assists with the study recruitment plan and provides input into the study budget; manages all screening, enrollment and study participation logs; completes recruitment summary at study termination.

Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management and record keeping; and conducts accurate and timely subject data collection,

Assists with study database development to maintain study data in de-identified format, according to recognized skill level; completes Case Report Forms (CRF’s) and ensures CRF’s are completed prior to monitor visits.

Educates other study personnel with regards to study-specific responsibilities and keeps written documentation of this training.

Alerts the investigator when the subject’s safety is in jeopardy, there is a protocol deviation, or when the subject requests premature study termination.

Responsible for regulatory/IRB issues after a study has been initiated; maintains regulatory binder.

Assists the principal investigator in the preparation of scientific publications and grant proposals.

Qualifications:
KNOWLEDGE, SKILLS AND ABILITIES REQUIRED:

 

Education:

BA/BS preferred; Associates degree or equivalent work-related experience required.

Required Experience:

CRA/CRC certification preferred.

Minimum of 18 months experience in clinical research or health care field, two years preferred.

Preferred Experience:

Understanding of medical terminology and clinical trials preferred.

Working knowledge of PCs and word processing and data management software.

Demonstrated analytical skills with accuracy and attention to detail.

Excellent verbal and written communication skills.

Goal-oriented and self-directive, ability to manage complex projects independently.

Strong organizational and interpersonal skills.

Ability to actively participate as a team player.

Minimum Physical Requirement:

Squat/kneelReaching above shoulder (Occasionally) 

Driving (Occasionally) 

Exposed to fumes/gases/vapors (Occasionally) 

Exposed to loud noises (Occasionally) 

Exposed to cold temperatures (Occasionally) 

Bend/twist (Frequently)

Standing (Frequently)

Walking (Frequently)

Sitting (Frequently)

Lifting/carrying up to 50 lbs. may need assistance Pushing/pulling up to 100 lbs. may need assistance (Frequently)

Exposed to blood and/or bodily fluids (Frequently)

Exposed to communicable diseases and/or pathogens (Frequently)

Exposed to chemicals/medicationsWork with patient equipment (Frequently)

EOE/M/F/Disability/Vet.

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