Houston Methodist
Research Coordinator II - Obstetrics and Gynecology Research
Houston Methodist, Houston, Texas, United States, 77246
Research Coordinator II - Obstetrics and Gynecology Research
The Research Coordinator II is responsible for coordinating the day-to‑day activities of research protocols, ensuring accurate data collection, documentation, organization, and safety of research participants. Under minimal supervision, the role gathers patient data, assesses patient eligibility, and performs general administrative duties supporting the study.
Education
Bachelor’s degree
Experience
Four years of research experience
Licenses & Certifications
Certified Clinical Research Coordinator (ACRP) or Certified Clinical Research Professional (SOCRA)
Skills & Abilities
Demonstrates required skills and competencies for safe job performance
Proficient in speaking, reading, and writing English, especially when it impacts safety or security
Communicates effectively with patients, physicians, family members, and coworkers using customer‑service language
Works independently and handles challenging situations
Demonstrates sound judgment and above‑average analytical skills
People Essential Functions
Drafts communications with sponsors and regulatory documents under PI direction
Identifies, recruits clinical research subjects, and monitors enrollment goals
Conducts in‑services and precepts new staff on study procedures
Takes a teaching role, encouraging critical thinking among peers and improving department metrics
Service Essential Functions
Participates in PI meetings
Schedules, coordinates, and participates in pre‑site and site initiation visits; obtains informed consent and documents it
Performs phlebotomy and monitors participants’ labs, notifying PI of findings
Quality/Safety Essential Functions
Prepares IRB documents, addressing stipulations for approval; documents IRB and contract approval
Maintains source documentation and appropriate forms per protocol; assists in quality assurance and adheres to internal controls
Finance Essential Functions
Assists with budget development and Medicare coverage analysis
Manages time effectively to prioritize work and achieve results
Growth/Innovation Essential Functions
Assists PI or research nurse in planning and designing source documents for protocol
Develops laboratory collection and storage procedures
Incorporates input from other health‑care disciplines into protocols and assists in eliciting data from external sources
Manages professional development and completes My Development Plan
Supplemental Requirements
On‑call:
Not required
Travel:
May require travel within Houston Metropolitan area: No; outside area: No
Work Attire:
Uniform: No; Scrubs: Yes; Business professional: No; Other (department approved): Yes
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Education
Bachelor’s degree
Experience
Four years of research experience
Licenses & Certifications
Certified Clinical Research Coordinator (ACRP) or Certified Clinical Research Professional (SOCRA)
Skills & Abilities
Demonstrates required skills and competencies for safe job performance
Proficient in speaking, reading, and writing English, especially when it impacts safety or security
Communicates effectively with patients, physicians, family members, and coworkers using customer‑service language
Works independently and handles challenging situations
Demonstrates sound judgment and above‑average analytical skills
People Essential Functions
Drafts communications with sponsors and regulatory documents under PI direction
Identifies, recruits clinical research subjects, and monitors enrollment goals
Conducts in‑services and precepts new staff on study procedures
Takes a teaching role, encouraging critical thinking among peers and improving department metrics
Service Essential Functions
Participates in PI meetings
Schedules, coordinates, and participates in pre‑site and site initiation visits; obtains informed consent and documents it
Performs phlebotomy and monitors participants’ labs, notifying PI of findings
Quality/Safety Essential Functions
Prepares IRB documents, addressing stipulations for approval; documents IRB and contract approval
Maintains source documentation and appropriate forms per protocol; assists in quality assurance and adheres to internal controls
Finance Essential Functions
Assists with budget development and Medicare coverage analysis
Manages time effectively to prioritize work and achieve results
Growth/Innovation Essential Functions
Assists PI or research nurse in planning and designing source documents for protocol
Develops laboratory collection and storage procedures
Incorporates input from other health‑care disciplines into protocols and assists in eliciting data from external sources
Manages professional development and completes My Development Plan
Supplemental Requirements
On‑call:
Not required
Travel:
May require travel within Houston Metropolitan area: No; outside area: No
Work Attire:
Uniform: No; Scrubs: Yes; Business professional: No; Other (department approved): Yes
#J-18808-Ljbffr