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
and protocols, may perform phlebotomy and other patient-oriented tasks, and may perform other related duties as requested or directed.
CHRISTUS Santa Rosa Hospital - Westover Hills (CSRH-WH) is a 150-bed hospital serving the fastest growing area of San Antonio.
Specialized care includes orthopedic and surgical services, ICU, women’s services, a newborn nursery, comprehensive cardiovascular care from diagnostics to open heart surgery, vascular lab, sleep center, emergency services, the CHRISTUS Weight Loss Institute, wound care, rehabilitation, and more. The campus also boasts an Outpatient Imaging Center and three medical plazas, one of which houses our CHRISTUS Santa Rosa Family
Medicine Residency Program and CHRISTUS Santa Rosa Family Health Center. Responsibilities: • Meets expectations of the applicable One CHRISTUS Competencies: Leader of Self, Leader of Others, or Leader of Leaders.
• Performs all routine and complicated laboratory procedures in the primary section to which assigned about age or interaction specific values. • Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary or notifies Bio-med as needed. • Must cross-train to other laboratory sections as needed. • Assures that the laboratory's quality control program is properly followed. • Calculates, enters, and/or verifies results of
laboratory procedures. • Utilizes the Laboratory Information System.
• Provides notification and documentation of critical laboratory values obtained. • Processes patient specimens, including collection, handling, and distribution always cognizant of minimal pediatric specimen volumes (when required). • Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. • Demonstrates competence to perform assigned patient care responsibilities in a manner that meets the population-specific and developmental needs of patients served by the department. • Appropriately adapts assigned patient backssment, treatment, and/or care methods to accommodate the unique physical, psychosocial, cultural, age specific and other developmental needs of each patient served.
• Demonstrates adherence to the CORE values of CHRISTUS Health. • Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. • Performs other duties as assigned. Requirements: Bachelor’s Degree or higher in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution or equivalent laboratory training and experience meeting the requirements defined in the CLIA regulation 42CFR493.1489 (includes U.
S. Military laboratory training courses of at least 50 weeks) OR Education that has been evaluated by an acceptable credentialing agency and deemed equivalent to a US Bachelor’s degree in a chemical, physical, biological or clinical laboratory science or medical technology. One year of experience required for graduates of a clinical laboratory training program approved or accredited by NAACLS, or other organizations approved by HHS. OR Two years of approved clinical laboratory experience, which must include a clinical rotation through the following sections of the laboratory: Blood Banking, Microbiology, Chemistry, and Hematology, Immunology, and Urinalysis/Body Fluids in the U.
S. or with an accredited laboratory within the last 5 years OR 5 years of experience as a Medical Laboratory Technician (MLT II cannot move to a CLS II). Must possess Certification for MT, MLS, CLS, or MLT from ASCP, AMT, AAB, or HEW/HHS. If certification with an expiration date is held, the certification must be maintained and kept current. New Graduate that is Board Certified or eligible (must complete Board Certification in 1 year of hire, Louisiana excluded) Work Schedule: PRN Work Type: Per Diem As Needed EEO is the law - click below for more information: www.
eeoc. gov/sites/default/files/2023-06/22-088_EEOC_Know Your Rights6.12Screen Rdr. pdf We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at (844) 257-xyz X. For more details: jobs-search. org/manufacturing_san-antonio-c448656/clinical-laboratory-scientist-ii-lab-admingeneral-prn-san-antonio_i1973476415
of researchers on research and development projects to accomplish technical goals. This offers a wonderful learning opportunity. Perform, analyze, and discuss the results with the team and design innovative solutions to solve technical challenges. The basic qualifications for this position are as follows: BS or MS in Chemistry, Materials Science, or Engineering Basic technical writing and presentation skills Ability to work in a multi-disciplinary team environment involving close interaction with scientists Candidates able to satisfy one or more of the following qualifications are preferred: Understanding of chemistry lab safety procedures.
Willingness to learn new science and work hard.
Candidates must submit a 1or 2-page resume highlighting their experience and education, especially as these would pertain to the qualifications and desired credentials mentioned above.
The position is open only until filled. Candidate must be a " US Person" (Citizen or Permanent resident) due to contract requirements. Interested candidates are encouraged to apply online at. Feel free to include a cover letter or expanded resume to outline how you fit this position. Lynntech is an Equal Opportunity Employer/M/F/Vet/Disabled. Job Posted by Applicant Pro
have exciting opportunities for a Research Assistant with a strong Molecular Biology background to participate in molecular assay development and testing. Responsibilities and prospects for professional career growth include, but are not limited to: Assisting in the experimental design and development of molecular assays Performing molecular studies, analyzing, and interpreting test results Maintaining a laboratory notebook as a detailed log of experiments, results, and ongoing research efforts Education and experience required: Bachelor's degree in the biological sciences (or a related field) Experience working in a molecular biology-oriented lab Experience in performing molecular techniques
that include, isolation of DNA/RNA, primer design, conventional PCR, real-time PCR , gel electrophoresis , ELISA, and western blot Experience in microbiology and/or cell biology is highly desired Ability to design and carry out experiments with limited supervision Excellent organizational and data management skills Proven technical writing abilities Effective communication (oral and written) skills that enable the individual to interact with all levels of management, technical and scientific personnel In our challenging and multidisciplinary work environment, qualified applicants will have the opportunity to develop their own scientific interests and broaden laboratory skills.
This profitable,
dynamic company offers an excellent compensation and benefits package.
Our facilities are located in College Station, Texas, just four miles from Texas A&M University. Qualified applicants should apply online at. Lynntech, Inc. is an Equal Opportunity Employer M/F/Vet/Disabled. Job Posted by Applicant Pro
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
