Apply now »
Title: Research Coordinator II - TCH Anesthesiology
Division: TCH Departments
Schedule: Monday – Friday, 8 a.m. – 5 p.m.
Work Location: Houston, TX
Salary Range: $44,948 - $51,683
FLSA Status: Nonexempt
Requisition ID: 18734
Summary
Coordinates day to day activities of clinical trial research studies for the TCH Pediatric Anesthesiology Department. Primary responsibilities include protocols which include patient enrollment, screening, monitoring of research participants, and reporting to the clinical research sponsor and Principal Investigators. The Research Coordinator II 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 at Texas Children’s Hospital to enroll and follow up on study patients.
Job Duties
- Interviews, screen and recruits patients for enrollment in studies.
- Performs the subject consent process of patients.
- Conducts subject research study education as required within the scope of practice.
- Collect and record study data related to individual studies.
- Collects patient information and enter into database.
- May collect, process, ship, and maintain paperwork for blood and/or biological specimens.
- Maintains records and regulatory documents and records for research studies.
- May assist with the supply orders and equipment necessary for the study.
- Interviews, screen and recruits patients for enrollment in studies; explains process and procedures to educate participant 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.
- Conducts subject research study education as required within the scope of practice.
- Discusses study protocols with patients and verifies the informed consent documentation.
- Responsible for assisting the Principal Investigator with collecting and/or recording study data related to individual studies. This may include pre/intra/postop vital signs, scales/scores for pain, nausea.
- 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 electronic medical chart abstractions; processes documents and enters information into databases or case report forms.
- Build and manage databases according to study protocols. Database entry can be through various methods and REDCap is the primary database at TCH.
- May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol.
- Maintains records and regulatory documents and records for research studies.
- Meets with Principal Investigators and Research Supervisor, operating independently, or with only minimal guidance.
- Submits serious adverse event reporting and follow up as needed.
- May assist with the supply orders and equipment necessary for the study.
- 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 duties as assigned.
Minimum Qualifications
- Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
- One year of relevant experience.
Preferred Qualifications
- Master's degree in a related field.
- One year of clinical research experience.
- Strong oral and written communication skills, ability to work on a team and independently; organized, takes initiative; professional, will communicate with staff, faculty, nursing staff, patients and families.
- Ability to adapt to the diverse departmental research needs.
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.
18734
Apply now »
Similar Positions
-
Clinical Studies Coordinator Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, United States, 7 days ago
The primary purpose of the Coordinator, Clinical Studies position is to collaborate with the research team and Principal Investigator (PI) to coordinate clinical trial subject accrual and data man...
-
Clinical Studies Coordinator Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, United States, 7 days ago
The Clinical Studies Coordinator collaborates with the research team and principal investigator in managing research protocols, assuring protocol compliance, quality assurance and communicating wi...
-
Research Data Coordinator Health Services Research English/Spanish, University of Texas MD Anderson Cancer Center, United States, 20 days ago
JOB SPECIFIC COMPETENCIES Recruitment • Screens individuals for study eligibility by reviewing charts or other data according to study protocols • Contacts individuals in person, by phone, email, ...
-
Coordinator, Clinical Studies Thoracic Head & Neck Medical Oncology, University of Texas MD Anderson Cancer Center, United States, 22 days ago
Coordinator, Clinical Studies - Thoracic-Head & Neck Medical Oncology The University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on cancer pa...
-
Director, Animal Care, Baylor College of Medicine, United States, 20 days ago
Summary The Center for Comparative Medicine (CCM) supports the animal oversight and research needs of all investigators utilizing animals in their research and teaching at Baylor College of Medici...
-
Coordinator, Clinical Studies Lymphoma Myeloma, University of Texas MD Anderson Cancer Center, United States, 21 days ago
Coordinator, Clinical Studies MISSION STATEMENT The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding p...