Clinical Research Coordinator - Spine

Overview

Come lead with us at Houston Methodist Academic Institute

At Houston Methodist, the Research Coordinator 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. This position ensures accurate data collection, documentation, organization and safety of research participants.

FLSA STATUS
Exempt

• Education
  Bachelor’s degree
• Experience
  Two years’ research experience
• 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
• Language
  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
• Communication
  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
• Data Entry
  Sufficient in clinical and research data entry
• Situational
  Capable of handling challenging/difficult situations
• Judgment
  Demonstrates sound judgment and executes analytical skills
• Note

• Under the direction of higher level staff, conducts screening and interviews to evaluate patient eligibility in study.
• Promotes a positive work environment and contributes to a dynamic, team focused work unit that actively helps one other to achieve optimal department results. Collaborates with all members of the patient care team by actively communicating and reporting pertinent information as it relates to assigned system(s) in a comprehensive manner.
• Provides contributions towards improvement of department scores for employee engagement.

• Responds promptly and accurately to customer complaints, inquiries, and requests for information and coordinate appropriate follow-up calls and/or appointments.
• Schedules research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol.
• Compiles patient information, process, document and enter accurate information in Source Documents, Case Report Forms, Electronic Data Capture portals and Clinical Trial Management System following established procedures.

• Maintains records for clinical study and regulatory documents.
• Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities.
• Assists management with research records and regulatory maintenance.

• Uses resources efficiently; does not waste supplies. Evaluates and reports on inventory levels. Self-motivated to independently manage time effectively and prioritize daily tasks.
• Maintains inventory of supplies necessary for the study.

• Maintains working knowledge of the research process and in the conduct of IRB approved research protocols. Follows International Conference on Harmonization (ICH)/Good Clinical Practice (GCP) guidelines.
• Seeks opportunities to expand learning beyond baseline competencies with a focus on continual development. Completes and updates My Development plan on an on-going basis.

• Uniform:
  No
• Scrubs:
  Yes
• Business professional:
  No
• Other (department approved):
  Yes

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