Senior Research Coordinator - Pediatrics - CRA Neurology Research

Baylor College of Medicine; Houston (TX); Sur place; USD 70 000 - 95 000; Plein temps

Résumé du poste

Baylor College of Medicine in Houston, TX seeks a Senior Research Coordinator to manage and oversee complex pediatric clinical trials within the Department of Pediatrics. You will handle enrollment, screening, drug dispensation per protocol, data collection, and safety reporting under FDA GCP guidelines.

Independent day-to-day operation and data integrity are essential. With strong regulatory knowledge and experience in CTMS, REDCap, Epic systems, and Excel, you will collaborate with clinicians,

Qualifications

• Bachelor's degree in a Basic Science or related field required; four years of related experience may substitute for degree.
• Five years of relevant experience preferred; strong clinical research background is essential.
• Experience in interventional clinical trials and regulatory compliance highly desirable.

Responsabilités

• Manage multiple studies in pediatrics clinical trials with regulatory compliance.
• Lead feasibility reviews including protocol logistics, staffing and resources.
• Oversee enrollment, screening, and informed consent processes with participants.
• Coordinate subject visits, education, and protocol adherence across teams.
• Collect, enter, and verify data; manage CTMS and safety reporting to sponsors.
• Prepare documentation for protocol approvals and regulatory submissions.

Connaissances

Interventional clinical trials

Independent work

Communication

Problem solving

Data management

Formation

Bachelor's degree in Basic Science or related field

Associate's degree or higher preferred

Outils

REDCap

Epic

CTMS

Microsoft Excel

Description du poste

Summary

The Senior Research Coordinator clinically and administratively manages multiple studies and complex clinical trials in the Department of Pediatrics, Center for Research Advancement. Primary responsibilities include patient enrollment, screening, monitoring of research participants, compliance, and reporting to the clinical research sponsor. The Senior Research Coordinator should be able to independently lead the day to day operations of a complex clinical research study, and will be responsible for ensuring accurate data collection, documentation, organization and safety of study volunteers. This position will be working directly with physicians and investigators to review treatment protocols and follow up on study patients. Candidates must have a working knowledge of FDA Good Clinical Practices, and the ability to read, analyze, and interpret information. The position requires prior clinical research experience and able to work independently with minimal oversight.

Job Duties

Clinically and administratively manages multiple studies involving rapid scale up and a high volume of patients/participants in a complex clinical trial. Leads and participates in study feasibility by completing a comprehensive review of protocol and study logistics such as staffing resources, patient population, and clinical resources needed to correctly conduct study.

Screening & Enrollment: 20% of Duties

• Interviews, screens and recruits patients for enrollment in studies.
• Explains process and procedures to educate participants regarding the research study.
• Performs the subject consent process of patients after verifying eligibility based on comprehensive inclusion and exclusion criteria outlined in the protocol.

Subject Visits: 30% of Duties

• Conducts subject research study education as required within the scope of practice.
• Discusses study protocols with patients and verifies the informed consent documentation.
• Dispenses study medication in a professional and accountable manner following protocol and hospital requirements.

Data Collection & Entry: 20% of Duties

• Responsible for assisting the Principle Investigator with collecting and recording study data related to cauterization procedures, cardiac measurements, and related test and measurement for the study.
• Collaborates with physician, mid-level practitioners, and research nurses and data managers to document patient care.
• Collects patient information through direct patient interviews, questionnaires and chart abstractions; processes documents and enters information into databases or case report forms.
• Responsible for electronic case reporting requirements in accordance with all FDA and clinical trial study requirements.
• Manages and enters study information into CTMS (clinical trial management system) database.

Other

Source Document/Document Review & Development: 15% of Duties

• Prepares documentation necessary to obtain initial and continued approval for the specific research protocol.
• Oversees study-related documentation. Reviews protocol documents, including abstracts, text, and informed consent for relevant information.
• Evaluates and analyzes clinical research data as appropriate. Generates reports and presents data analysis.

Communication with Sponsor/Subjects/PI's: 15% of Duties

• Meets with Principal Investigators and Study Sponsors, operating independently, or with only minimal guidance.
• Interacts with sponsors and/or coordinating sites as required to facilitate protocol activities and maintains current study documents.
• Submits serious adverse event reporting and follow up as needed.
• Adheres to FDA Good Clinical Practices outlining the standard for safety, design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trials or studies
• Adheres to Baylor College of Medicine, Texas Children's Hospital and Clinical Research SOPs
• Performs other job duties as assigned.

Minimum Qualifications

• Bachelor's degree in a Basic Science or related field. Four years of related experience may substitute for degree requirement.
• Five years of relevant experience.

Preferred Qualifications

• Minimum 5 years of experience in interventional clinical trials.
• Associate's degree or higher required.
• Experience with complex clinical trial coordination, including study startup, participant visits, protocol implementation, and regulatory compliance.
• Experience with AE/SAE reporting strongly preferred.
• Knowledge of REDCap, Epic, CTMS, and Microsoft Excel preferred.
• Strong data management and documentation skills.
• Ability to work independently while collaborating with investigators and research teams.
• Comfortable working in a fast-paced research environment with multiple active studies.
• Flexible schedule and willingness to support study activities outside standard business hours when required.
• Experience managing study data, regulatory requirements, and clinical trial documentation.
• Strong communication, organizational, and problem-solving skills.

Work Authorization Requirement:

This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.