Clinical Research Coordinator I, Oncology

Posted 17 Hours Ago
Be an Early Applicant
Orange, CA, USA
In-Office
29K-49K Hourly
Junior
Healthtech
The Role
Under moderate supervision, coordinate oncology clinical research: assess protocol feasibility, prepare IRB submissions, identify and consent participants, collect data/specimens, maintain study records, support QA audits, manage supplies, communicate with teams, and archive study documentation.
Summary Generated by Built In

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

Under moderate supervision, the Clinical Research Coordinator I (CRC-I) is expected to perform all core Clinical Research Coordinator (CRC) responsibilities for human subjects’ (clinical) research. Study management includes but is not limited to assisting in assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, 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-I may also be responsible for development of source documents and/or case report forms and coordination of research/project team meetings. The CRC-I is the second position in the Clinical Research Coordinator series.

Pay Range

Minimum $29.48 Midpoint $39.04 Maximum $48.61

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 one (1) year 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.

Specialized Skills

Required: Basic knowledge of key Microsoft Office programs (Word, Excel, PowerPoint). Able to communicate effectively both orally and in writing. Demonstrate strong interpersonal skills. 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 six (6) months of assuming position. With management approval, the time in which to obtain certification may be extended past six (6) months due to extenuating circumstances.

Preferred: Phlebotomy certification.

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.

Skills Required

  • Minimum one (1) year of clinical research coordination experience.
  • Associate degree or equivalent additional experience (acceptable in lieu of education).
  • Basic knowledge of Microsoft Office programs (Word, Excel, PowerPoint).
  • Working knowledge of human subjects regulatory requirements and ICH-GCP.
  • Able to communicate effectively orally and in writing; strong interpersonal skills.
  • Detail oriented and able to manage multiple competing priorities in a fast-paced environment.
  • RQI Responder - American Heart Association certification (must obtain within six months if not currently held).
  • Clinical research experience in a hospital setting and/or pediatric clinical research experience.
  • Bachelor's degree.
  • Ability to conduct informed consent.
  • Working knowledge of Cerner or equivalent electronic medical record system.
  • Knowledge of sample identification, processing, and storage.
  • Phlebotomy certification.
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The Company
5,234 Employees
Year Founded: 1954

What We Do

Rady Children’s Health is a nonprofit pediatric healthcare system dedicated to advancing children’s health through compassionate care, innovative treatments, and leading-edge research. The organization includes Rady Children’s Hospital San Diego and a broader network of hospitals, primary and specialty care centers, trauma centers, and health services supporting children and families across Southern California and beyond.

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