← Back to jobs
Full-time

Clinical Research Coordinator II, Critical Care

Competitive

Orange, CAScience & PharmaceuticalPosted 21d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Location

Orange, CA

Posted

21 days ago

Job description

Children’s Hospital of Orange County is hiring a Clinical Research Coordinator II to support multiple human subjects clinical research projects. The role manages study feasibility, regulatory submissions, participant identification, data and specimen collection, study records, quality assurance, materials, team communication, and record archiving.

Tags

Health Care

Social Media

Education

Wellness

Healthcare

Communities

Fitness

Insider Connection @CHOC Children's

2 email credits available today

Beyond your network

Lisa Stofko & 4 connections

From your previous company

Responsibilities

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

Preferred

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

Bachelor's degree in a relevant field

Ability to conduct informed consent

Working knowledge of Cerner or equivalent electronic medical record system

Knowledge of sample identification, processing and storage

Phlebotomy certification

Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC)

Glassdoor

4.1

Bringing compassion, innovation, and worldclass pediatric care so children have the chance to turn their brightest dreams into reality.

Orange, California, USA

http://www.choc.org/

Late Stage

Total Funding

$2M

Key Investors

Baldrick's Foundation

Tsao Family Foundation

2025-01-08

Acquired

Qualifications

Minimum three years of clinical research coordination experience

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

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)

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

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

Bachelor's degree in a relevant field

Ability to conduct informed consent

Working knowledge of Cerner or equivalent electronic medical record system

Knowledge of sample identification, processing and storage

Phlebotomy certification

Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC)

Minimum three years of clinical research coordination experience.

Required skills

Clinical Research Coordination, Human Subjects Regulatory Requirements, ICH-GCP, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, RQI Responder (American Heart Association), Informed Consent, Cerner, Specimen Identification, Processing, and Storage, Phlebotomy Certification, ACRP-CP, CCRP, or CCRC Certification

Preferred skills

Bachelor's degree in a relevant field, Ability to conduct informed consent, Knowledge of sample identification, processing and storage, Phlebotomy certification, Glassdoor, 4.1, Orange, California, USA, http://www.choc.org/, Late Stage, Total Funding, $2M, Key Investors, Baldrick's Foundation, Tsao Family Foundation, 2025-01-08, Acquired, 2023-11-21, Grant, 2022-06-01, Grant· $2M, Leadership Team, Kimberly Cripe, President and CEO, Kim Milstien, Chief Operating Officer, Recent News, HealthCareIT News, AI's promise meets the pediatric frontline, 2026-05-23, PR Newswire

Experience

3+ years

Interested in this role?

Apply directly on the employer's website — it only takes a few minutes.

Similar vacancies

Other roles in Orange, CA or Science & Pharmaceutical

HealthcareFull-time
San FranciscoScience & PharmaceuticalsPosted 30+ Days Ago

You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…

HealthcareFull-time
USA - Torrance (205th Street)Science & PharmaceuticalPosted 25d ago

When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.

HealthcareFull-time
BIDMC East CampusScience & PharmaceuticalPosted 26d ago

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.