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, Humanities, Women's, Gender & Sexuality Studies, 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 is responsible for coordinating day-to-day activities of research protocols, including CHAP follow-up studies and sponsored clinical trials. Key duties include overseeing participant screening, enrollment, and monitoring to ensure adherence to study protocols. This role ensures accurate and timely collection, documentation, and organization of data and specimens, while prioritizing the safety and well-being of research participants. Additionally, this position develops and implements effective recruitment strategies to engage participants in long-term clinical research studies.
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 perform Venipuncture (blood draws), EKGs/ECG’s and obtain vital signs on study participants.
- Receive on the job training of phlebotomy and EKGs/ECGs prior to performing on study participants.
- Maintains records and regulatory documents and records for research studies.
- Schedule research participant for tests and procedures such as laboratory tests, x-rays, and other studies specific for the research protocol.
- May correspond with patient throughout study.
- Keeps all required trainings and certificates up to date.
- 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.
- One year of experience working in clinical trials with human subjects.
- Bilingual (English and Spanish).
- EPIC and database experience.
- Medical background and terminology.
- Excellent communication skills.
- Able to communicate with vulnerable population.
- Keeps calm in urgent situations.
- Ability to multi-task is critical to this role.
Requisition ID: 21365
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