Houston Methodist•2h ago
Career Pages
Research Coordinator I
Houston, TX
Full Time
Mid Level
N/A
N/A
N/A
Qualifications
8/8 matched
Experience Level: Mid Level
- Bachelor's degree
- Two years' 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
- Sufficient in clinical and research data entry
- Capable of handling challenging/difficult situations
- Demonstrates sound judgment and executes analytical skills
Full Job Description
As a vital academic institute dedicated to groundbreaking research, Houston Methodist seeks a Research Coordinator I. This role is integral to the daily operations of research protocols, ensuring participant safety and the meticulous collection of research data. The position involves actively screening and interviewing potential participants to confirm eligibility for studies.
Key Responsibilities:
- Evaluate patient eligibility through screening and interviews for study participation.
- Foster a positive and collaborative work environment, contributing to a dynamic team that supports mutual achievement of departmental goals.
- Communicate effectively with the entire patient care team, providing comprehensive and timely updates on relevant patient information.
- Address customer complaints, inquiries, and information requests promptly and accurately, coordinating necessary follow-up actions.
- Schedule appointments for research subjects for essential tests and procedures, including laboratory work, imaging, and protocol-specific studies.
- Compile patient data, process information, and accurately document and enter it into source documents, case report forms, electronic data capture portals, and clinical trial management systems according to established procedures.
- Maintain comprehensive records for clinical studies and regulatory documentation.
- Report Adverse Events (A/E) and Serious Adverse Events (SAE) to appropriate regulatory authorities under the guidance of the Research Nurse, Clinical Trial Manager, or Physician.
- Support management in maintaining research records and regulatory compliance.
- Utilize resources efficiently, minimizing waste and monitoring inventory levels. Demonstrate self-motivation and effective time management skills to prioritize daily tasks.
- Manage and maintain an inventory of necessary study supplies.
- Stay current with research processes and the execution of IRB-approved research protocols, adhering to International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines.
- Actively pursue opportunities for professional development and continuous learning, updating personal development plans regularly.
Qualifications:
- Bachelor's degree required.
- Minimum of two years of research experience.
- Demonstrated skills and competencies for safe job performance, validated through ongoing assessments and evaluations.
- Proficiency in English (speaking, reading, writing) sufficient to perform essential job functions, particularly those impacting patient or employee safety.
- Effective communication skills with patients, physicians, family members, and colleagues, demonstrating a customer service focus and positive language principles.
- Proficiency in clinical and research data entry.
- Ability to manage challenging and difficult situations effectively.
- Strong judgment and analytical skills.
Company
Houston Methodist
Houston Methodist stands as a premier healthcare institution in the United States, recognized for its leadership in health systems and academic medical centers.
Houston, TX
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