Assistant Clinical Research Coordinator
Evolution Research Group•Doral, FL
•$0 - $29•Onsite
About The Position
The Assistant Coordinator participates in clinical research studies conducted by the Clinical Research Coordinator. They assist and perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data.
Requirements
- Maintains current licensure, registration and/or certification within educational background
- Maintains current BLS and/or ACLS certification
- Maintains necessary CEU’s for licensure, registration and/or certification
- Actively participates on CPMI’s ongoing Quality Assurance Program, HIPAA and Compliance Programs
- Keeps apprised of all new OSHA and GCP/ICH rules and regulations
- Attends all appropriate team meetings regarding study protocols
- Maintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs
- Reads and understands CPMI policy and procedures manuals, SOP manual and employee handbook
Responsibilities
- Monitor and ensure study data is collected following plan of care, guidelines and identified group resources
- Serve in rotation with assistant clinical coordinators and clinical research coordinators
- Serve as liaison between assigned clinical research coordinator and all clinical departments
- Participate in collaborative team efforts with other departments
- Discuss and administer Informed Consent Form
- Check and ensure that procedure areas are properly stocked with study supplies and equipment (i.e. blood tubes, kits, study flowsheets, ECG machines, BP cuffs, etc.)
- Assist assigned Clinical Research Coordinator review study schedules to ensure that study procedures are properly staffed
- Assist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements
- Anticipate, recognize, and resolve issues
- Reads and understands each protocol in which she/he is involve
- Follow established guidelines in the collection of clinical data and/or administration of clinical studies
- Performs all other duties as assigned
- Support adverse event reporting and informed consent administration
- Notify staff of abnormal results or incidents
- Ensure participant comfort and readiness for procedures
- Set up supplies and procedure areas per protocol
- Perform venipuncture, vital signs, ECG, and other assessments
- Communicate with participants to explain procedures and gather data
- Assist with patient care and emergency measures as needed
- Attend study initiation meetings and perform study-related tasks
- Provide high-quality care under pressure
- Maintains current licensure, registration and/or certification within educational background
- Maintains current BLS and/or ACLS certification
- Maintains necessary CEU’s for licensure, registration and/or certification
- Actively participates on CPMI’s ongoing Quality Assurance Program, HIPAA and Compliance Programs
- Keeps apprised of all new OSHA and GCP/ICH rules and regulations
- Attends all appropriate team meetings regarding study protocols
- Maintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs
- Reads and understands CPMI policy and procedures manuals, SOP manual and employee handbook
Benefits
- medical and dental coverage
- a matching 401(k)
- paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
