Houston Methodist
Research Coordinator II - Cancer Clinical Trials
Houston Methodist, Houston, Texas, United States, 77246
Research Coordinator II - Cancer Clinical Trials
Come lead with us at Houston Methodist Academic Institute. At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study. Ideal applicants must possess strong analytical and problem-solving skills, as well as the proven ability to build rapport and foster communication with study participants and team members. People Essential Functions
Under the direction of the Principal Investigator (PI), drafts various communications with the Sponsor and/or regulatory documents to be sent to the Sponsor. Identifies and recruits clinical research subjects and monitors enrollment goals. May conduct in-services to floor nurses/physicians; assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies. Teaches peers to critically think by verbally expressing rationale for decisions and follows up consistently. Service Essential Functions
Participates in the Principal Investigator (PI) meetings. Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation. Obtains Informed Consent from study participant and documents appropriately. Obtains vital signs and performs phlebotomy per training and competence; monitors participants' labs and notifies the PI of laboratory findings. Quality/Safety Essential Functions
Prepares Institutional Research Board (IRB) documents under the direction of the PI, assists with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval. Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. Finance Essential Functions
Assists with the budget development and Medicare coverage analysis. Utilizes resources effectively and efficiently, demonstrating responsible financial stewardship. Growth/Innovation Essential Functions
Assists PI and/or research nurse in the planning and design of source documents for protocol. Assists in developing procedures for laboratory collection and storage. Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility. Proactively manages own professional development and completes My Development Plan. Education and Experience
Bachelor's degree Four years of research experience Licenses And Certifications
CCRC - Certified Clinical Research Coordinator (ACRP) OR CCRP - Certified Clinical Research Professional (SOCRA) preferred Knowledge, Skills, And Abilities
Demonstrates the skills and competencies necessary to safely perform the assigned job. Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job. Ability to effectively communicate with patients, physicians, family members and co-workers. Ability to work independently and handle challenging situations. Houston Methodist is an Equal Opportunity Employer.
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Come lead with us at Houston Methodist Academic Institute. At Houston Methodist, the Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study. Ideal applicants must possess strong analytical and problem-solving skills, as well as the proven ability to build rapport and foster communication with study participants and team members. People Essential Functions
Under the direction of the Principal Investigator (PI), drafts various communications with the Sponsor and/or regulatory documents to be sent to the Sponsor. Identifies and recruits clinical research subjects and monitors enrollment goals. May conduct in-services to floor nurses/physicians; assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies. Teaches peers to critically think by verbally expressing rationale for decisions and follows up consistently. Service Essential Functions
Participates in the Principal Investigator (PI) meetings. Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation. Obtains Informed Consent from study participant and documents appropriately. Obtains vital signs and performs phlebotomy per training and competence; monitors participants' labs and notifies the PI of laboratory findings. Quality/Safety Essential Functions
Prepares Institutional Research Board (IRB) documents under the direction of the PI, assists with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval. Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. Finance Essential Functions
Assists with the budget development and Medicare coverage analysis. Utilizes resources effectively and efficiently, demonstrating responsible financial stewardship. Growth/Innovation Essential Functions
Assists PI and/or research nurse in the planning and design of source documents for protocol. Assists in developing procedures for laboratory collection and storage. Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility. Proactively manages own professional development and completes My Development Plan. Education and Experience
Bachelor's degree Four years of research experience Licenses And Certifications
CCRC - Certified Clinical Research Coordinator (ACRP) OR CCRP - Certified Clinical Research Professional (SOCRA) preferred Knowledge, Skills, And Abilities
Demonstrates the skills and competencies necessary to safely perform the assigned job. Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job. Ability to effectively communicate with patients, physicians, family members and co-workers. Ability to work independently and handle challenging situations. Houston Methodist is an Equal Opportunity Employer.
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