Experience

Arizona Research Center

• United States
• Research Services
• 1 - 100 Employee

• Inpatient Team Manager & Clinical Research Coordinator

  • Apr 2022 - Present

  United States

• Clinical Research Coordinator

  • Oct 2016 - Present

  Phoenix, Arizona Area  Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.  Reviews and comprehends the protocol.  Attends investigator meetings as required or requested by the PI.  Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment… Show more  Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.  Reviews and comprehends the protocol.  Attends investigator meetings as required or requested by the PI.  Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.  Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials  Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.  Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.  Coordinates participant tests and procedures.  Collects data as required by the protocol. Assures timely completion of Case Report Forms.  Maintains study timelines.  Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor  Leads studies and team to manage the day to day activities of the study including problem solving, communication and protocol management.



ADOBE CLINICAL RESEARCH, LLC

• United States
• Medical Practices
• 1 - 100 Employee

• Clinical Research Coordinator

  • May 2014 - Oct 2016

  Tucson, Arizona Area  Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.  Reviews and comprehends the protocol.  Attends investigator meetings as required or requested by the PI.  Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment… Show more  Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures.  Reviews and comprehends the protocol.  Attends investigator meetings as required or requested by the PI.  Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.  Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials  Assists PI in communication of study requirements to all individuals involved in the study. Provides appropriate training and tools for study team members. Documents date of training and signatures of study personnel trained on study specific training log.  Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.  Coordinates participant tests and procedures.  Collects data as required by the protocol. Assures timely completion of Case Report Forms.  Maintains study timelines.  Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor Show less