Clinical Research Coordinator II

Job Summary

Required Qualifications

• •Minimum 1 year of research experience in health services or related fields
• •Bachelor's Degree
• •Bilingual in Spanish
• •focus in healthcare, public health, behavioral health, social work, or related field
• •Computer experience with Microsoft Office and/or other database management software
• •Exceptional interpersonal, organizational, and research interviewing skills
• •ability to effectively prioritize multiple tasks
• •Reliability and the ability to follow detailed research protocols with precision
• •Strong attention to detail
• •professional communication skills
• •capacity to manage several responsibilities simultaneously
• •Must be able to lift 50 lbs
• •Must be available for weekend shifts
• •Valid driver's license
• •Must provide proof of work authorization and eligibility to work
• •Must be a citizen or national of the United States, a lawful permanent resident, or a foreign national authorized to work in the United States without the need of an employer sponsorship
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to recruit, screen, select, determine eligibility and enroll trial participants
• •Must be able to collect more complex information
• •Must be able to perform medical assessments
• •Must be able to answer varied questions under supervision of a medically licensed professional
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to ensure participants follow the research protocol
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends
• •Must be able to schedule and coordinate study team meetings
• •Must be able to coordinate and support research studies conducted by the Pediatric Hospital Medicine and Complex Care Research Team
• •Must be able to perform participant-facing activities
• •Must be able to manage study operations
• •Must be able to coordinate data
• •Must be able to communicate with investigators and multi-site partners
• •Must be able to serve as the primary point of contact for clinical research participants, study investigators, and multi-stie collaborators
• •Must be able to ensure studies are conducted in accordance with study protocols, regulatory requirements, and institutional standards
• •Must be able to work in-person, onsite, at a designated campus work location
• •Must be able to work remotely, at an offsite, non-campus work location
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends
• •Must be able to schedule and coordinate study team meetings
• •Must be able to coordinate and support research studies conducted by the Pediatric Hospital Medicine and Complex Care Research Team
• •Must be able to perform participant-facing activities
• •Must be able to manage study operations
• •Must be able to coordinate data
• •Must be able to communicate with investigators and multi-site partners
• •Must be able to serve as the primary point of contact for clinical research participants, study investigators, and multi-stie collaborators
• •Must be able to ensure studies are conducted in accordance with study protocols, regulatory requirements, and institutional standards
• •Must be able to work in-person, onsite, at a designated campus work location
• •Must be able to work remotely, at an offsite, non-campus work location
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends
• •Must be able to schedule and coordinate study team meetings
• •Must be able to coordinate and support research studies conducted by the Pediatric Hospital Medicine and Complex Care Research Team
• •Must be able to perform participant-facing activities
• •Must be able to manage study operations
• •Must be able to coordinate data
• •Must be able to communicate with investigators and multi-site partners
• •Must be able to serve as the primary point of contact for clinical research participants, study investigators, and multi-stie collaborators
• •Must be able to ensure studies are conducted in accordance with study protocols, regulatory requirements, and institutional standards
• •Must be able to work in-person, onsite, at a designated campus work location
• •Must be able to work remotely, at an offsite, non-campus work location
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends
• •Must be able to schedule and coordinate study team meetings
• •Must be able to coordinate and support research studies conducted by the Pediatric Hospital Medicine and Complex Care Research Team
• •Must be able to perform participant-facing activities
• •Must be able to manage study operations
• •Must be able to coordinate data
• •Must be able to communicate with investigators and multi-site partners
• •Must be able to serve as the primary point of contact for clinical research participants, study investigators, and multi-stie collaborators
• •Must be able to ensure studies are conducted in accordance with study protocols, regulatory requirements, and institutional standards
• •Must be able to work in-person, onsite, at a designated campus work location
• •Must be able to work remotely, at an offsite, non-campus work location
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends
• •Must be able to schedule and coordinate study team meetings
• •Must be able to coordinate and support research studies conducted by the Pediatric Hospital Medicine and Complex Care Research Team
• •Must be able to perform participant-facing activities
• •Must be able to manage study operations
• •Must be able to coordinate data
• •Must be able to communicate with investigators and multi-site partners
• •Must be able to serve as the primary point of contact for clinical research participants, study investigators, and multi-stie collaborators
• •Must be able to ensure studies are conducted in accordance with study protocols, regulatory requirements, and institutional standards
• •Must be able to work in-person, onsite, at a designated campus work location
• •Must be able to work remotely, at an offsite, non-campus work location
• •Must be able to perform medical assessments after completion of required training/certification
• •Must be able to collect vital signs
• •Must be able to obtain weight
• •Must be able to perform phlebotomy
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to assist with training of staff
• •Must be able to schedule logistics
• •Must be able to determine workflows
• •Must be able to secure resources for clinical research trials
• •Must be able to perform quality checks
• •Must be able to identify resource needs and develop clinical research documents
• •Must be able to contribute to the development of protocols
• •Must be able to serve as a main point of contact for clinical research participants
• •Must be able to provide information regarding research procedures, expectations, and informational inquiries
• •Must be able to ensure participants follow the research protocol
• •Must be able to alert Principal Investigator of issues
• •Must be able to identify work unit resources needs and manage supply and equipment inventory levels
• •Must be able to manage research workflow components
• •Must be able to collect, prepare, process, and submit participant data and samples to appropriate entities
• •Must be able to adhere to research protocols
• •Must be able to perform participant recruitment and screening in inpatient and outpatient settings
• •Must be able to administer interviews and surveys
• •Must be able to collect and document data
• •Must be able to track participant stipends