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Clinical Research Coord II, Research Administration
full-timeIrvine$0k - $0k

Summary

Location

Irvine

Salary

$0k - $0k

Type

full-time

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About this role

Work Location

Orange, California


Work Shift

Day – 08hrs (United States of America)

Why CHOC?

At CHOC, we strive to be the leading destination of children’s health by providing exceptional and innovative care. We are responsible for the overall health of our community’s pediatric population in our hospitals, clinics, and practices. And because of our breadth of care, your career at CHOC can be as diverse and fulfilling as you determine. CHOC’s compensation structure, benefits offerings, and career development programs are geared to helping you achieve your professional and personal goals. Apply now to see where your career at CHOC can take you.

Environmental Sustainability Statement

Driven by the connection between children's health and a healthy environment, we commit to creating a healthcare model that incorporates environmental sustainability aligned with our mission to protect children's health and patient safety.

Job Summary

With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Study management includes but is not limited to assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, coordinating and collecting research data/specimens, completing study records in an accurate and timely manner, participating in quality assurance audits, managing study materials and supplies, communicating across multiple teams, and archiving records in accordance with appropriate policies and procedures. The CRC-II is the mid-level position in the Clinical Research Coordinator series.

Pay Range

Minimum $30.94 Midpoint $40.99 Maximum $51.05

Rate of pay is determined by various factors, including but not limited to knowledge, skills, competencies, experience, education, as well as position requirements.

Experience

Required: Minimum three years of clinical research coordination experience.

Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research experience.


Education 

Required: Associate degree or equivalent additional experience can be accepted in lieu of education.

Preferred: Bachelor’s degree in a relevant field.


Specialized Skills

Required: Basic knowledge of key Microsoft Office programs (Word, Excel, PowerPoint). Demonstrate strong interpersonal skills. Able to communicate effectively both orally and in writing. Be detail oriented.

Able to work under pressure in a fast-paced environment while managing multiple competing priorities. Working knowledge of human subjects’ regulatory requirements, and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Guidelines for Good Clinical Practice (ICH-GCP).

Preferred: Ability to conduct informed consent. Working knowledge of Cerner or equivalent electronic medical record system. Knowledge of sample identification, processing and storage.


Licensure

Required: RQI Responder- American Heart Association.  If incumbent does not have certification at time of hire or promotion, certification is expected to be obtained within 6 months of assuming position. With management approval, the time in which to obtain certification may be extended past 6 months due to extenuating circumstances.

Preferred: Phlebotomy certification. Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC).

Work Environments - Functional Demand:

Light - Moderate energy level Lift and carry 25-35 lbs. Push/pull 50-100 lbs. (ie. empty bed, stretcher).

Physical Activity Requirements:

Bending, Carry Objects, Climbing, Keyboard use/repetitive motion, Pinching/fine motor activities, Push/Pull, Reaching forward, Reaching overhead, Sitting, Squat/kneel/crawl (Squad & Knee), Standing, Talk or hear, Taste or smell, Twisting, Walking, Wrist position deviation

Physical Activity Lifting

Lifting (Floor to waist level) - Constant 67 or more%, Lifting (Floor to waist level) - Frequent 36-66%, Lifting (Floor to waist level) - Occasional 0-35%, Lifting (Waist level and above) - Constant 67 or more%, Lifting (Waist level and above) - Frequent 36-66%, Lifting (Waist level and above) - Occasional 0-35%

Sensory Requirements:

Color Discrimination, Depth Perception, Far Vision, Hearing, Near Vision

Environment Requirements:

Airborn Communicable Disease, Bloodborne Pathogens, Chemical, Dust Particular Matter, Extreme Noise Levels, Extreme Temperatures, Radiation, Uneven Surfaces or Elevations

Non-Discrimination Statement:

CHOC does not discriminate on the basis of age, race, color, religion, national origin, ancestry, marital status, genetic information, disability, sex, gender (including pregnancy, breastfeeding, childbirth, lactation or related medical conditions), gender identity or expression, medical condition, sexual orientation, veteran status, military or uniformed service member status, or other protected characteristics in accordance with state and federal laws. CHOC will consider for employment qualified applicants with criminal histories, in accordance with the Fair Chance Initiative for Hiring.

We encourage individuals from all backgrounds to apply for positions at CHOC, even if your experience doesn’t align perfectly with the listed qualifications for a particular role, as your unique experience may be a great addition to our culture for another one of our opportunities.

If you desire support or accommodations throughout the Talent Acquisition process, please inform your Talent Acquisition Partner.

Other facts

Tech stack
Clinical Research Coordination,Regulatory Requirements,Data Collection,Interpersonal Skills,Communication Skills,Detail Oriented,Quality Assurance,Microsoft Office,Study Management,Feasibility Assessment,Participant Identification,Record Keeping,Informed Consent,Electronic Medical Records,Sample Processing,Phlebotomy

About CHOC

Affiliated with the University of California, Irvine, CHOC's growing pediatric healthcare system is comprised of premier facilities, leading-edge programs and services, life-saving research, healing amenities, and education and training programs designed to prepare the next generation of pediatric experts.

Our mighty brigade of physicians, nurses and staff—each sharing a deep connection to our mission— are dedicated to caring for children, whether they’re healthy or seriously ill. So, kids can get back to being kids.

Team size: 1,001-5,000 employees
LinkedIn: Visit
Industry: Hospitals and Health Care
Founding Year: 1964

What you'll do

  • The Clinical Research Coordinator II is responsible for providing support to multiple clinical research projects, including managing study materials, coordinating data collection, and ensuring compliance with regulatory requirements. This role requires effective communication across teams and participation in quality assurance audits.

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Frequently Asked Questions

What does CHOC pay for a Clinical Research Coord II, Research Administration?

CHOC offers a competitive compensation package for the Clinical Research Coord II, Research Administration role. The salary range is USD 0k - 0k per year. Apply through Clera to learn more about the full compensation details.

What does a Clinical Research Coord II, Research Administration do at CHOC?

As a Clinical Research Coord II, Research Administration at CHOC, you will: the Clinical Research Coordinator II is responsible for providing support to multiple clinical research projects, including managing study materials, coordinating data collection, and ensuring compliance with regulatory requirements. This role requires effective communication across teams and participation in quality assurance audits..

Why join CHOC as a Clinical Research Coord II, Research Administration?

CHOC is a leading Hospitals and Health Care company. The Clinical Research Coord II, Research Administration role offers competitive compensation.

Is the Clinical Research Coord II, Research Administration position at CHOC remote?

The Clinical Research Coord II, Research Administration position at CHOC is based in Irvine, California, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Clinical Research Coord II, Research Administration position at CHOC?

You can apply for the Clinical Research Coord II, Research Administration position at CHOC directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about CHOC on their website.