Note: The job is a remote job and is open to candidates in USA. Houston Methodist is one of the nation’s leading health systems and academic medical centers. The Research Coordinator II position is responsible for coordinating the day-to-day activities of research protocols and ensuring accurate data collection and participant safety in clinical research studies.

Responsibilities

• 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. Uses peer-to-peer accountability towards improvement of department score for turnover/retention/employee engagement
• 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
• 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. Adheres to internal controls established for the department
• Assists with the budget development and Medicare coverage analysis
• Utilizes resources effectively and efficiently, demonstrating responsible financial stewardship. Manages own time effectively and prioritizes work to achieve maximum results in a timely manner
• 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; assists in eliciting relevant data from sources outside of the hospital
• Proactively manages own professional development and completes My Development Plan

Skills

• Bachelor's degree
• Four years of research experience
• Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations
• Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
• Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
• Ability to work independently
• Capable of handling challenging/difficult situations
• Demonstrates sound judgment and executes above average analytical skills
• CCRC - Certified Clinical Research Coordinator (ACRP)
• CCRP - Certified Clinical Research Professional (SOCRA)

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