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Research Coordinator II
full-timeHouston

Summary

Location

Houston

Type

full-time

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About this role

FLSA STATUS
Exempt

QUALIFICATIONS

EDUCATION
  • Bachelor’s degree

EXPERIENCE
  • Four years of research experience

LICENSES AND CERTIFICATIONS
Preferred
  • CCRC - Certified Clinical Research Coordinator (ACRP) or
  • CCRP - Certified Clinical Research Professional (SOCRA)

SKILLS AND ABILITIES
  • 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


ESSENTIAL FUNCTIONS

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. Uses peer-to-peer accountability towards improvement of department score for turnover/retention/employee engagement.

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. Adheres to internal controls established for the department.

FINANCE ESSENTIAL FUNCTIONS
  • 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.

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; assists in eliciting relevant data from sources outside of the hospital.
  • Proactively manages own professional development and completes My Development Plan.


SUPPLEMENTAL REQUIREMENTS
    WORK ATTIRE
    • Uniform: No
    • Scrubs: Yes
    • Business professional: No
    • Other (department approved): Yes

    ON-CALL
    Note that employees may be required to be on-call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below.
    • On Call* No

    TRAVEL
    Travel specifications may vary by department**
    • May require travel within the Houston Metropolitan area No
    • May require travel outside Houston Metropolitan area No

Other facts

Tech stack
Research Experience,Communication Skills,Analytical Skills,Patient Interaction,Clinical Research,Regulatory Knowledge,Time Management,Team Collaboration,Problem Solving,Phlebotomy,Informed Consent,Quality Assurance,Budget Development,Professional Development,Education,Recruitment

About Houston Methodist

Houston Methodist is one of the nation’s leading health systems and academic medical centers. The health system consists of eight hospitals: Houston Methodist Hospital, its flagship academic hospital in the Texas Medical Center, seven community hospitals and one long-term acute care hospital throughout the Greater Houston metropolitan area. Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care, emergency care and imaging centers; and outpatient facilities. Houston Methodist employs more than 32,000 people. Come lead with us.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Hospitals and Health Care

What you'll do

  • The Research Coordinator II assists the Principal Investigator in drafting communications, recruiting clinical research subjects, and monitoring enrollment goals. They also prepare IRB documents, manage source documentation, and assist with budget development.

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Frequently Asked Questions

What does a Research Coordinator II do at Houston Methodist?

As a Research Coordinator II at Houston Methodist, you will: the Research Coordinator II assists the Principal Investigator in drafting communications, recruiting clinical research subjects, and monitoring enrollment goals. They also prepare IRB documents, manage source documentation, and assist with budget development..

Why join Houston Methodist as a Research Coordinator II?

Houston Methodist is a leading Hospitals and Health Care company.

Is the Research Coordinator II position at Houston Methodist remote?

The Research Coordinator II position at Houston Methodist is based in Houston, Texas, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Research Coordinator II position at Houston Methodist?

You can apply for the Research Coordinator II position at Houston Methodist directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Houston Methodist on their website.