Clinical Research Coord II, Oncology
About The Position
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.
Requirements
- Minimum three years of clinical research coordination experience
- 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
- Working knowledge of International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Guidelines for Good Clinical Practice (ICH-GCP)
- Basic Life Support (BLS) - American Heart Association certification (or obtained within 6 months of hire)
- Lift and carry 25-35 lbs
- Push/pull 50-100 lbs
- 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
- Color Discrimination
- Depth Perception
- Far Vision
- Hearing
- Near Vision
Nice To Haves
- Clinical research experience in a hospital setting
- 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)
Responsibilities
- 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
- Archiving records in accordance with appropriate policies and procedures
Benefits
- CHOC’s compensation structure, benefits offerings, and career development programs are geared to helping you achieve your professional and personal goals.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
