Clinical Research Coordinator

We are more than a health system. We are a belief system. We believe wellness and sickness are both part of a lifelong partnership, and that everyone could use an expert guide. We work hard, care deeply and reach further to help people uncover their own power to be healthy. We inspire hope. We learn, grow, and achieve more – in our careers and in our communities.Job Description Summary:The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. This position performs basic day to day activities related to clinical research studies including: recruit and screen participants, obtains informed consent, educate participants regarding study requirements, event reporting, collection of and organizes research data and complete case report forms. This position applies basic level of understanding to the ability to perform a variety of tasks under direct supervision in a range of different type of clinical studies.Responsibilities And Duties:Study Planning and CoordinationAssists with implementation and coordination of research studies and projects.Accountable to PI for study specific responsibilities.Works closely with PI and direct supervisor to organize, plan and carry out the research in an efficient and timely manner.Assists with protocol feasibility, resource requirements and study planning activities including leading internal training to implement the protocol and avoid deviations.Assists with recruitment procedures for potential participants and oversees the enrollment of the clinical trial as directed by the PI.Ensures that study parameters are correctly applied prior to a research participant enrolling in a study and during the research participant’s visits and assessments.Extracts and records physical findings, laboratory data and other details essential to each study onto the required data collection forms accurately and within the designated timeAttends investigator’s meetings, pre-study site visits which may require travel, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.Participates in in-house protocol meetings to review study-related procedures, staffing and visit flow.Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant’s responsibilities in the study.Responsible for giving participant instructions and serves as the primary contact for subjects by being available to handle study specific questions, concerns or events.Accurately records and extracts data from source documentation onto required data collection forms (paper or electronic) in a timely manner. Maintains accurate and timely source documentation.Prepares study documents for archiving according to timelines, following closeout visits activitiesResponsible for in-depth knowledge of protocol requirements and GCP guidelines.Performs other related duties as assigned or required.Patient CareAssists nursing and clinical staff and applies skills and knowledge to facilitate the care of research participants.Assists nursing and clinical staff and utilizes knowledge of disease processes to observe, report adverse events, and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.Quality and ComplianceAssists in audit preparedness activities for OHRI.Assists with monitoring visits on site or remotely and is available during visits for corrections, questions, etc.Maintains study records according to sponsor and/or regulations.Keep records in a secure location.ReportingAssist in the development of reporting metrics.Generates reports and reviews to ensure validity of data.Provide ad hoc reports.CommunicationDemonstrates effective communications skills.Communicates information in a timely and accurate manner.Functions as a liaison with sponsor and investigator regarding the preparation, execution and completion of studies.Adapts communication skills in response to various situations including those related to differences in culture, age, education and other communication barriers.Uses various media forms to maximize communication success.Demonstrates teamwork characteristics.Ability to manage time, prioritize and follow up on projects as necessary taking into consideration the need for flexibility when working on multiple projects.Participates in meetings with OHRI, PI and clinical teams to review patient status at a detailed level.Works with research staff to effectively communicate patient process for each trial for the life of the study.Advise, communicate and reinforce standard practices, regulations to following regarding research study participation.OtherAttends relevant training courses on policy and compliance.Ensures assigned training is complete and meets internal qualifications.Responsible for completing all necessary training for their position.Maintain familiarity with evolving regulatory and compliance context.Other duties as assigned.As a High Reliability Organization (HRO), responsibilities require focus on safety, quality and efficiency in performing job duties.The job profile provides an overview of responsibilities and duties and is not intended to be an exhaustive list and is subject to change at any timeMinimum Qualifications:Bachelor's Degree (Required)Additional Job Description:Degree required from a four year college or universitySPECIALIZED KNOWLEDGEAbility to prioritize assigned workStrong verbal and written communication skills, as well as customer service skills and ability to problem solve, prioritize and manage multiple tasksStrong computer skills, including thorough knowledge of systems (EMR, Microsoft)DESIRED ATTRIBUTESOne year of relevant work or academic experience preferredPrior experience in a medical environment preferredClinical Research Coordinator Certification (or equivalent approved Clinical Research Certification)One or more years of direct human subjects researchClinical knowledge in assigned therapeutic area or programMAJOR DUTIES/RESPONSIBILITIES & ESSENTIAL FUNCTIONSStudy Planning and CoordinationAssists with implementation and coordination of research studies and projects.Accountable to PI for study specific responsibilities.Works closely with PI and direct supervisor to organize, plan and carryout the research in an efficient and timely manner.Assists with protocol feasibility, resource requirements and study panning activities including leading internal training to implement the protocol and avoid deviations.Assist with recruitment procedures for potential participants and oversee the enrollment of the clinical trial as directed by the PI.Ensures that study parameters are correctly applied prior to a research participant enrolling a study and during the research participant’s visits and assessments.Extracts and records physical findings, laboratory data and other details essential to each study onto the required data collection forms accurately and within the designated time periodAttends investigator’s meetings, pre-study site visits which may require travel, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.Participate in in-house protocol meetings to review study-related procedures, staffing and visit flow.Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant’s responsibilities in the study.Responsible for giving participant instructions and serves as the primary contact for subjects by being available to handle study specific questions, concerns or events.Accurately records and extracts data from source documentation onto report forms (paper or electronic) in a timely manner. Maintains accurate and timely source documentation.After closeout visits have been conducted, prepares study documents for archiving according to timelines.Responsible for in-depth knowledge of protocol requirements and GCP guidelines.Performs other related duties as assigned or required.Patient CareAssists nursing and clinical staff and applies skills and knowledge to facilitate the care of research participants.Assists nursing and clinical staff and utilizes knowledge of disease processes to observe and report adverse events and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.Quality and ComplianceAssists in audit preparedness activities for OHRI.Assists with monitoring visits on site and is available during visits for corrections, questions, etc.Maintains study records according to sponsor and/or regulations.Keep records in a secure location.ReportingAssist in the development of reporting metrics.Generates reports and reviews to ensure validity of data.Provide ad hoc reports.CommunicationDemonstrates effective communications skills.Communicates information in a timely and accurate manner.Functions as a liaison with sponsor and investigator regarding the preparation, execution and completion of studies.Adapts communication skills in response to various situations including those related to differences in culture, age, education and other communication barriers.Uses various media forms to maximize communication success.Demonstrates teamwork characteristics.Ability to manage time, prioritize and follow up on projects as necessary taking into consideration the need for flexibility when working on multiple projects.Participates in meetings with OHRI, PI and clinical teams to review patient status at a detailed level.Work with research staff to effectively communicate patient process for each trial for the life of the study.Advise, communicate and reinforce standard practices, regulations to following regarding research study participation.OtherAttends relevant training courses on policy and compliance.Ensures assigned training is complete and meets internal qualifications.Responsible for completing all necessary training for their position.Maintain familiarity with evolving regulatory and compliance context.Other duties as assigned.Work Shift:DayScheduled Weekly Hours :40DepartmentOncology Research Clinical ServicesJoin us!... if your passion is to work in a caring environment... if you believe that learning is a life-long process... if you strive for excellence and want to be among the best in the healthcare industryEqual Employment OpportunityOhioHealth is an equal opportunity employer and fully supports and maintains compliance with all state, federal, and local regulations. OhioHealth does not discriminate against associates or applicants because of race, color, genetic information, religion, sex, sexual orientation, gender identity or expression, age, ancestry, national origin, veteran status, military status, pregnancy, disability, marital status, familial status, or other characteristics protected by law. Equal employment is extended to all person in all aspects of the associate-employer relationship including recruitment, hiring, training, promotion, transfer, compensation, discipline, reduction in staff, termination, assignment of benefits, and any other term or condition of employment #J-18808-Ljbffr OhioHealth