FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Clinical Research Coordinator I, Orthopedics
CHOCClinical Research Coordinator I working under moderate supervision performing core clinical research responsibilities at CHOC. Involves managing study protocols, participant identification, data collection, and quality assurance audits.
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Perform all core Clinical Research Coordinator (CRC) responsibilities for human subjects’ (clinical) research.
- 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.
- Archiving records in accordance with appropriate policies and procedures.
- Development of source documents and/or case report forms.
- Coordination of research/project team meetings.
Requirements
What you’ll need- Minimum one (1) year of clinical research coordination experience.
- Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research experience.
- Associate degree or equivalent additional experience can be accepted in lieu of education. Preferred: Bachelor’s degree.
- 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 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.
Benefits
Comp & perks- CHOC’s compensation structure, benefits offerings, and career development programs are geared to helping you achieve your professional and personal goals.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Clinical Research CoordinationData CollectionRegulatory Submission PreparationQuality Assurance AuditsSource Document DevelopmentSample IdentificationProcessing and StorageFeasibility AssessmentStudy Record ManagementCase Report Form Development
Soft Skills
Effective CommunicationInterpersonal SkillsDetail OrientedAbility to Work Under PressureTime Management