Clinical Research Coordinator II (CRC)
- $23 to $27 Hourly
- Medical , Dental , Paid Time Off , Retirement
- Full-Time
This position is responsible for performing highly diverse clinical and administrative responsibilities requiring a high level of knowledge and attention to detail. This position requires assimilating vast amounts of information and processing information promptly and orderly. Personnel who fill this role must have a working knowledge of ICH/GCP guidelines. Specific studies are assigned as appropriate, and the coordinator is accountable to the Principal Investigator, Medical Director, and Clinical Research Manager.
Qualifications
- 1+ years of previous experience required as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials
- Computer skills - Microsoft Word, Excel, PowerPoint, CTMS, EMR
- Previous experience in a role of complex administration or project coordination
- Effective communication skills, including written, verbal, and presentation skills
- Strong attention to detail and organizational, analytical, and problem-solving skills
- Periodic local travel to other practice locations on an as-needed basis
Supervisory Responsibilities
This position may serve a role in supporting/ mentoring junior coordinators and research assistants
Job Duties/Responsibilities
- Ensure the rights, safety and welfare of all subjects at all times
- Ensure that each subject goes through the informed consent process following GCP guidelines, and consents to participate, before any study-related procedures are performed
- Work in a collaborative, effective manner with the Sponsor personnel to meet research objectives completely and accurately
- Work in a collaborative, effective manner with Site personnel to meet research objectives completely and accurately
- Responsible for understanding all internal policies and procedures approved by the Principal Investigator/Medical Director
- Discuss study protocols with patients and verify informed consent documentation
- Review patient medical history against Inclusion/Exclusion Criteria of studies
- Perform blood draws, process and shipping of blood/urine specimens per study protocol and IATA regulations
- Schedule all patient research visits and procedures consistent with protocol requirements
- Dispense study medication, collect vital signs, and perform ECGs
- Assist with routine data verification and quality control, ensuring data integrity and consistency with the prescribed study protocol
- Provide the Sponsor with accurate and complete documentation and information
- Provide accurate and complete documents for IRB submission on a timely basis
- Complete and maintain accurate, legible and complete source documents and case report forms per FDA guidelines and Sponsor requirements
- Retain and/or forward copies of forms as required by the Sponsor
- Inform Sponsor of prospective FDA audits immediately
- Prepare for FDA or Sponsor audit by ensuring all documentation and case report forms are available and complete
- Provide subject education on an ongoing basis throughout their participation in the study
- Report all adverse events to the Investigator, Sponsor and IRB.
- Complete Study Logs in an accurate and timely manner in the appropriate electronic data system
- Utilize a team approach including the PI, Sub-Investigators, other Coordinators and Research Assistant
- Assist in the training of new staff members
- Other duties as assigned
Address
DLCFL
100 N Dean Rd
Orlando, FLIndustry
Healthcare
Posted date
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