Clinical Research Coor RN - Direct Patient Care

Nationwide Children's Hospital Inc; Columbus (OH); Hybrid; USD 65,000 - 85,000; Full time

Job summary

Nationwide Children's Hospital is seeking a Clinical Research Coordinator RN - Direct Patient Care at Main Campus in Columbus, OH. You will partner with study physicians to manage patient care within clinical trials, ensuring adherence to GCP and regulatory requirements while safeguarding participant safety.

Required BSN or associate degree with plans to obtain BSN within 5 years, Ohio RN license, CPR certification; NRP/PALS preferred.

Qualifications

• BSN or ASN with commitment to obtain BSN within 5 years is required.
• Ohio RN license is required.
• CPR certification is required; NRP and PALS preferred.

Responsibilities

• Plans, educates, and evaluates care plan using evidence-based practices according to the study protocol.
• Provides nursing care with a family-centered approach while ensuring safety and quality in trial participation.
• Communicates patient care needs to all involved providers to facilitate positive outcomes in clinical care and trial participation.
• Manages procedural, regulatory, and training elements to ensure participant safety and data integrity.

Skills

Nursing skills

Venipuncture

IV starts

Data management

Verbal communication

Team player

Organizational skills

Education

BSN or ASN with commitment to obtain BSN within 5 years

Tools

Data management software

PC literacy

Job description

## Clinical Research Coor RN - Direct Patient CareApply: Main Campus, Columbus, OH: Full time: Posted Today: R-28006**Overview:****Job Description Summary:**Works with the study physician to ensure all patients involved in a clinical research trial are managed uneventfully, safely, and as effectively as possible through their episode of care and participation in the clinical research trial, ensuring patient care is not compromised while participating in the trial. Manages all elements of a clinical research trial in order to meet all protocol obligations while following applicable regulations; Code of Federal Regulations Good Clinical Practices (GCP) and International Conference on Harmonization GCP guidelines; state regulations and departmental/institutional standard operating procedures.**Job Description:****Essential Functions:*** Plans, implements, educates and evaluates care plan using Evidence-Based Practices in accordance with the requirements of the study protocol* Provides nursing care using a Family Centered approach throughout their clinical study participation while maintaining quality and safety as a priority. Delegates, directs, oversees and provides developmentally appropriate patient care. Practices professional nursing and promotes patient advocacy in accordance with the ANA Code of Ethics for Nurses and maintains a current Ohio Nursing License* Collaborates effectively and communicates patient care needs/expectations/priorities related to clinical trial participation to all involved care providers including unit nursing staff, attending physician, ancillary service providers (radiology, cardiology, physical therapy, pharmacy, etc.) to facilitate positive patient outcomes both in clinical care and in clinical trial participation* Completes and manages all procedural, data, regulatory and training elements associated with clinical research project implementation, execution and close out to ensure participant safety, data integrity and compliance with all applicable regulations.**Education Requirement:**BSN or Associate's Degree with commitment to obtain BSN within 5 years of hire, required.**Licensure Requirement:**Registered Nurse in the State of Ohio, required.**Certifications:*** CPR, required.* Obtain and maintain NRP and PALS certification as determined by management.* Certification by the Association of Clinical Research Professionals or Society of Clinical Research Administrators, preferred.**Skills:*** Demonstrated proficiency in clinical nursing skills, (i.e.: venipuncture, IV starts and injections);* Understanding of medical terminology, clinical trials preferred* Working knowledge of PCs, word processing, and data management software* Strong verbal, written, interpersonal communication* Goal-oriented; self-directive, initiation, self-motivation, creativity, flexibility* Excellent organizational, attention to detail and prioritization skills* Ability to actively participate as a team player**Experience:**Clinical research experience, preferred.**Physical Requirements:**OCCASIONALLY: Bend/twist, Biohazard waste, Blood and/or Bodily Fluids, Chemicals/Medications, Climb stairs/ladder, Cold Temperatures, Color vision, Communicable Diseases and/or Pathogens, Depth perception, Driving motor vehicles (work required) \\*additional testing may be required, Electricity, Flexing/extending of neck, Fume /Gases /Vapors, Hand use: grasping, gripping, turning, Hot Temperatures, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Lifting / Carrying: 41-60 lbs, Lifting / Carrying: 61-100 lbs, Loud Noises, Patient Equipment, Peripheral vision, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 100 lbs or greater with assistance, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Pushing / Pulling: 61-100 lbs, Reaching above shoulder, Seeing – Far/near, Squat/kneelFREQUENTLY: Decision Making, Interpreting Data, Problem solving, Standing, WalkingCONTINUOUSLY: Audible speech, Computer skills, Hearing acuity, Repetitive hand/arm use, Sitting\"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet\"