Research Coordinator II : Pediatrics : Hematology and Oncology Clinical Research | Houston, TX

effort to develop new concepts and biologics to treat diseases related to over-nutrition. Currently, our focused research areas are: 1) The gap junction-dependent and -independent functions of the Connexin43 protein in adipocyte metabolism, adipokine secretion, milk production, and the communication of adipocytes with other types of cells within the depot.

We apply basic scientific discoveries to develop biologics that concurrently engage adipocyte metabolism and gap junction activity to improve the efficacy of the starting molecule. (Cell Metab. 2016, 24, 420–433, and APSB. 2022, In Press); 2) Hyaluronic acid (HA) production, hepatic clearance, and its role in modulating metabolism and

liver fibrogenesis. We place a special emphasis on the effects of HA in modulating the immune function of the liver during the pathogenesis of nonalcoholic steatohepatitis (NASH) and its role in intrahepatic communication among hepatic sinusoidal endothelial cells, Kupffer cells, and stellate cells.

(Sci. Trans Med. 2016, 8, 323ps4, Matrix Biol. 2019, 78-79, 284-291, and Nat. Commun. 2021, 12 (1), 1-15. ) Job Duties Plans, directs, and conducts research experiments. Evaluates and analyzes data, manage on-line data repositories. Manages related technical staff for operation of the animal colony. Redeploy new existing techniques for experiments and performs applications required for specific

research projects. Assists in completion and publication of ‘orphan’ lab projects.

Oversees the maintenance of lab equipment and environment. Coordinates and completes administrative duties such as ordering, computer assignments, organization, etc. Minimum Qualifications Bachelor's degree in a Basic Science or a related field. Two years of relevant experience. Preferred Qualifications Master's degree in basic science or a related field with a minimum of one year of research experience. Please provide unofficial transcripts.

day to day activities of research protocols for the Epidemiology program and supporting all research efforts of the program. Daily activities that include screening, enrollment, and monitoring of research participants as well as ensuring accurate data collection, documentation, organization and safety of research participants.

The Coordinator should have excellent communication skills, since study participants can be recruited in person, via phone, or email. Research coordinator will also be responsible for completing all relevant study documents, maintaining research charts, providing study updates, and completing study progress reports. Job Duties Interviews, screen and recruits patients

for study; explains process and procedures to educate participant regarding the research study. Ensures research protocol objectives are being met and research activities meet institutional and regulatory standards.

Collects patient information. Processes documents and enters information into a database. Collects, processes, ships, and maintains paperwork for specimens according to procedures outlined in study protocol. Maintains records and regulatory documents for research studies. Organizes study research documents following specific protocol guidelines. Corresponds with patients throughout study. Works in a team environment with faculty and other staff members to ensure protocol objectives

are being met. Schedules study meetings and conference calls.

Prepares study meeting agendas, participate in meetings, and track meeting minutes/notes. 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. Two years of relevant experience. Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer. 18101

of the Principal Investigator and Clinical Research Manager, the ideal candidate will perform assigned activities related to clinical research studies. The ideal candidate will be an experienced clinical research coordinator highly driven, self-motivated and eager to work both independently as well as be part of a dynamic team.

Candidate should have the ability to evaluate a patient's medical record for eligibility and recruitment. Candidate must have excellent verbal, written, and interpersonal communication skills. Must be reliable, detail oriented, have advanced organizational and planning skills as well as be people-oriented. Must have the ability to assist with multiple projects

and manage time effectively. Must be flexible and have an understanding that their job description and responsibilities can change as the role is developed.

Job tasks will include but not be limited to: · Review of patient's records to screen for eligibility· Call potential patients to discuss study· Schedule/ Reschedule appointments for study patients· Prepare patient charts· Assist with input of clinical exams into EDC· Assist with clinical exams as needed· Assist with collection of required paperwork· Correspond with PCPs as necessary· Assist with end of study paperwork· Phlebotomy skills· Screening backssmentsa Qua Research Institute, LLC. offers a competitive wage & benefits package

for full-time eligible employees that includes: Medical Insurance Vision Insurance Dental Insurance 401(k) Life Insurance & Short and Long-Term Disability PTO Job Type: Full-time Pay Rate starting: $25.00Ability to commute/relocate: Houston, TX 77058: Reliably commute or planning to relocate before starting work (Required) Experience: Clinical Research Coordinator: 3 years (Preferred) Phase II - IV in-patient/out-patients clinical studies Job Posted by Applicant Pro

will be part of an interdisciplinary team of researchers led by Dr. Amy Mc Guire, the Leon Jaworski Professor of Medical Ethics and Director of the Center for Medical Ethics and Health Policy. This is a hybrid position and will be based in Houston, TX.

The start date for this position is flexible. Candidates finishing master’s degree programs in Spring 2024 are encouraged to apply. In addition to supporting the Center’s robust research program, the Clinical Research Associate will have the opportunity to participate in professional and academic development sessions hosted by the Center. Such development opportunities include speaker series, grand rounds and peer mentorship. The Center

promotes an intellectually stimulating and collaborative environment conducive to academic excellence. The Center for Medical Ethics and Health Policy cultivates a culture of intentionality, respect, inclusivity, and collaboration.

We offer intellectual, social, and professional development opportunities to promote a meaningful work experience. We are reflective and mindful of issues related to diversity, equity and inclusion in both interactions with one another. For more information about Baylor College of Medicine and the Center for Medical Ethics and Health Policy, visit our website at www. bcm. edu/ethics. Job Duties Provide daily research support for ongoing projects, including

organizing project files, scheduling project activities and meetings, taking meeting minutes, and coordinating with co-investigators, collaborators, and project personnel across multiple sites to move projects forward.

Coordinate recruitment and enrollment for study participants. Maintain project databases, including collecting and tracking data and reporting on project components to ensure timelines are adhered to and deadlines are met. Assist with quantitative research data coordination and management, for example, contributing to instrument development and refinement, programming surveys instruments, executing data collection, data cleaning and quality control oversight, and creating data visualizations in Excel.

Maintain manuals of procedure for projects and oversees study-related documentation. Conduct comprehensive literature searches in the areas of bioethics, social science, health policy and biomedical sciences. Assist with document preparation and references for publications and new project proposals. Attend project meetings. Perform other job-related duties as assigned. Minimum Qualifications Bachelor's degree. Two years of relevant experience. Preferred Qualifications Master's degree in bioethics, humanities, public health, social sciences or related field.

Master’s degree can be accepted in lieu of experience requirement. Strong interest in bioethics, health policy, genomics, neuroethics, public health, and/or related issues. Experience with data management and quantitative methodologies. Experience with data analysis software programs (e. g. Excel, SPSS, STATA). Ability to display a professional, positive attitude with strong interpersonal skills and communication skills required and must be able to work independently and collaboratively to meet deadlines. Team oriented, collaborative mindset with an interest in creating value in any situation with insightful questions and suggestions.

Detail-oriented, self-motivated, efficient, and strong organizational skills. Demonstrate a high degree of flexibility in accepting work assignments with the ability to effectively prioritize tasks, understand processes, and resolve issues. Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer. 18105