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Research Coordinator - Orthopedics Clinical

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Houston Methodist
Full Time position
Listed on 2026-01-12
Job specializations:
  • Science
    Clinical Research
Job Description & How to Apply Below
Position: Research Coordinator I - Orthopedics Clinical

Research Coordinator I - Orthopedics Clinical

Join us at Houston Methodist to lead and coordinate the day‑to‑day activities of research protocols, ensuring accurate data collection, documentation, and the safety of research participants.

FLSA Status

Exempt

Qualifications Education
  • Bachelor’s degree
Experience
  • Two years’ research experience
Licenses and Certifications
  • Required:

    none specified
Skills and Abilities
  • Demonstrates the skills and competencies necessary to safely perform the assigned job as determined through ongoing assessments.
  • Sufficient proficiency in speaking, reading, and writing the English language necessary for patient or employee safety and security.
  • Effective communication with patients, physicians, family members, and co‑workers, maintaining a customer‑service focus.
  • Clinical and research data entry proficiency.
  • Ability to handle challenging or difficult situations.
  • Sound judgment and analytical skills.
Essential Functions People
  • Conducts screening and interviews to evaluate patient eligibility in the study under supervision.
  • Promotes a positive work environment and collaborates with the patient care team to communicate and report pertinent information.
  • Contributes to improving department scores for employee engagement.
Service
  • Responds promptly and accurately to customer complaints, inquiries, and requests, coordinating follow‑up calls or appointments.
  • Schedules research subject appointments for tests and procedures such as laboratory tests, x‑rays, and other study‑specific tests.
  • Compiles, processes, documents, and enters accurate information in Source Documents, Case Report Forms, Electronic Data Capture portals, and Clinical Trial Management System according to established procedures.
Quality/Safety
  • Maintains records for clinical studies and regulatory documents.
  • Captures and reports Adverse Events (AE) or Serious Adverse Events (SAE) to regulatory authorities under supervision.
  • Assists management with research records and regulatory maintenance.
Finance
  • Uses resources efficiently, evaluates inventory levels, and self‑manages time to prioritize daily tasks.
  • Maintains inventory of supplies necessary for the study.
Growth/Innovation
  • Maintains working knowledge of the research process and IRB‑approved protocols, following ICH/GCP guidelines.
  • Seeks opportunities for continual learning, completing and updating a development plan regularly.
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 (e.g., disaster, severe weather events) regardless of the current selection.
  • On Call:
    No
Travel
  • Travel specifications may vary by department.
  • May require travel within the Houston Metropolitan area:
    No
  • May require travel outside the Houston Metropolitan area:
    No
Seniority Level

Entry level

Employment Type

Full‑time

Job Function

Research, Analyst, and Information Technology

Industries

Hospitals and Health Care

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