Research Coordinator II - Obstetrics & Gynecology
- Employer
- Baylor College of Medicine
- Location
- Houston, Texas, United States
- Salary
- Competitive Salary
- Date posted
- Jan 16, 2025
View more categoriesView less categories
- Position Type
- Faculty Positions, Health Sciences, Other Health & Medicine, Administrative, Academic Affairs, Research Administration
- Employment Type
- Full Time
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Summary
This position is located within the field of Clinical Research in the OB/GYN department. Our department is covering the OB/GYN services at two hospitals (TCH PFW and BTGH). We are conducting dozens of high-quality clinical research studies on both sites with million dollars internal and external fundings. We are working diligently to help promoting women's health in multiple levels. This position coordinates day to day activities of research protocols which include screening, enrollment, and monitoring of research participants. Also ensures accurate data/specimen collection, documentation, organization and safety of research participants.
This position also serves as a study site leader to lead the site team and provides training and support as needed. This position may require after-hour and weekend work. If you are asked to work during these times, your hours will be adjusted accordingly the following week.
Job Duties
- Screens, recruits, and interviews patients for study; explains process and procedures to educate participant regarding the research study.
- Collects patient information from interviews and EPIC; processes documents and enters information into a computerized database.
- Collects, processes, and transports the blood/biological specimens according to procedures outlined in study protocol; maintain paperwork for specimens.
- May correspond with patient throughout study.
- Keeps all required trainings and certificates up to date.
- Serves as a study site leader to lead the site team and provides training and support as needed
- After-hour and weekend on call may be needed.
- Performs other job duties as assigned.
- Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
- One year of relevant experience.
- Master's degree in a related field.
- Bilingual (English and Spanish).
- Two or more years of experience working in clinical trials with human subjects.
- EPIC and database experience.
- Medical background and terminology.
- Excellent communication skills.
- Ability to multi-task is critical to this role.
- Skills to communicate with vulnerable population.
- Keeps calm in urgent situations.
Requisition ID: 21364
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