Market Range: 10
Hiring Salary: $4,182.12 - $5,000.00/Monthly
THIS IS A GRANT-FUNDED POSITION FUNDED UNTIL JULY 1, 2027. THE FUNDING MAY BE EXTENDED PENDING FUNDING AVAILABILITY.
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Study Coordinator 2 plans, directs, and coordinates activities related to clinical research in the Department of Obstetrics & Gynecology. This position is responsible for understanding research protocols and regulatory guidelines and accurately completing research tasks in order to achieve the goals of the projects and the department.
MINIMUM REQUIREMENTS:
EDUCATION: Bachelor's Degree. (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years related experience; OR a combination of education and experience to equal six (6) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
WORK SCHEDULE: This position may occasionally be required to work weekends and evenings. May require occasional overnight travel.
Submits new protocols for institutional approval bodies and observes reporting requirements of these bodies throughout the study.
Assists in study planning and development, including protocol development, creating study forms, and mediating budget and contract communications.
Conducts and documents surveys, patient interviews, or observational data per protocol requirements.
Creates and maintains study logs for effective trial management; maintains regulatory documents and study communications in the appropriate projects critical documents binder.
Coordinates daily study activities and communicates with study personnel to ensure adequate staff coverage for protocol and regulatory requirements
Learns the protocols and procedures of each study as assigned and be prepared to perform delegated duties as required by the protocol
Monitors and documents adverse events, protocol deviations, and barriers to success.
Trains clinical or research staff to specific research protocols as indicated or assigned.
Performs or assists with the collection, documentation, processing and shipping of lab samples
Abstracts patient health information for entry into research data collection forms.
Completes required training certifications (CITI, IATA, lab safety, etc.) and comply to relevant guidelines
Performs other duties as assigned.
Submits new protocols for institutional approval bodies and observes reporting requirements of these bodies throughout the study.
Assists in study planning and development, including protocol development, creating study forms, and mediating budget and contract communications.
Conducts and documents surveys, patient interviews, or observational data per protocol requirements.
Creates and maintains study logs for effective trial management; maintains regulatory documents and study communications in the appropriate projects critical documents binder.
Coordinates daily study activities and communicates with study personnel to ensure adequate staff coverage for protocol and regulatory requirements
Learns the protocols and procedures of each study as assigned and be prepared to perform delegated duties as required by the protocol
Monitors and documents adverse events, protocol deviations, and barriers to success.
Trains clinical or research staff to specific research protocols as indicated or assigned.
Performs or assists with the collection, documentation, processing and shipping of lab samples
Abstracts patient health information for entry into research data collection forms.
Completes required training certifications (CITI, IATA, lab safety, etc.) and comply to relevant guidelines
Performs other duties as assigned.