Clinical Research Coordinator II - Oncology

Benefits

Qualifications

• •Required: Minimum three years of clinical research coordination experience
• •Required: Associate degree or equivalent additional experience can be accepted in lieu of education
• •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)
• •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
• •Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC)
• •Light - Moderate energy level 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
• •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%
• •Color Discrimination, Depth Perception, Far Vision, Hearing, Near Vision
• •Airborn Communicable Disease, Bloodborne Pathogens, Chemical, Dust Particular Matter, Extreme Noise Levels, Extreme Temperatures, Radiation, Uneven Surfaces or Elevations
• •19 more items(s)

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