Heart Failure Prevention Clinical Research Study (El Dorado)

AMR Clinical Layton Research Center is now enrolling people ages 12 and up in a clinical research study for those diagnosed with hidradenitis suppurativa (HS). HS is a chronic skin condition that causes painful lumps and abscesses. Qualified participants must: Have been diagnosed with HS for at least 6 months Have mild to moderate HS Have at least four nodules or abscesses, no draining tunnels, and symptoms in at least two areas such as the underarms, groin, or under the breast meet other study criteria Qualified participants will receive all study-related care and investigational medication at no cost. Compensation is available up to $1,700.00 for study-related time and travel. If you're interested in learning more about this trial, you can reach out to AMR today by calling 801-955-3700 or visiting their website at amrlayton.com for more detailed information.

Struggling with Stage 3Type 1 Diabetes? Take Part in Our Clinical Trial! Stage 3 Type 1 Diabetes is when the disease becomes active, and symptoms are noticeable. By this point, the immune system has destroyed most of the pancreas’s insulin-producing cells, causing high blood sugar. Symptoms often include frequent urination, extreme thirst, weight loss, fatigue, and blurry vision. Insulin therapy is required immediately to manage blood sugar and prevent serious health issues. We’re currently conducting a clinical study to explore potential new treatments for people living with this condition improving blood sugar control and enhancing overall well-being. Participants will receive study-related care, medication at no cost, and may be eligible for compensation. We are seeking volunteers for a clinical study to assess the safety and Stage 3Type 1 Diabetes. If you or someone you know may be interested, please contact us to learn more about eligibility and potential benefits. Plus, refer a friend who qualifies and earn a BONUS of $100! Call 828-579-2273 Now! Or Apply Here Why Participate? Compensation: Get compensated up to $100 per clinic visit with no cost to you or your insurance! Comprehensive Support: Regular check-ins and assessments to ensure your health is a priority. Our trial is conducted by experienced healthcare professionals dedicated to your well-being. Free study medications: Study medications for Stage 3 Type 1 Diabetes are given at no cost. To qualify: *18 years old and above *Diagnosed with Type 1 Diabetes Check out our other studies! * Moderate to Severe Plaque Psoriasis * Thyroid Eye Disease * Future Studies Asheville Clinical Research Your participation can help advance Type 2 Diabetes research and improve lives. If you're ready to take action, contact us at 828-579-2273 or visit Asheville Clinical Research website for more information. Get Involved Today!

Ocean Associates Inc. (OAI) is seeking applicants for a full-time position to support the NOAA/NMFS Office of International Affairs, Trade, and Commerce (IATC), Highly Migratory Species (HMS) Trade Monitoring Program as a Process Control Officer. OAI is a Virginia corporation established in 2003 that provides consulting and technical services to the U.S. government, non-governmental organizations, international organizations, and the private sector. We specialize in scientific program and project management, strategic planning, professional and technical services and stakeholder engagement, supporting government contracts. NOTE: A cover letter that describes how your skills, experience and education meet the required qualifications of the position must be included with your resume when submitting the application and is mandatory Description: The NOAA/NMFS conducts the Highly Migratory Species (HMS) Trade Monitoring Program for Atlantic and Pacific Bluefin Tuna, Bigeye Tuna, Southern Bluefin tuna, and Swordfish. These species are regulated both internationally as well as domestically under various international agreements and domestic legislation. The United States and NMFS are specifically obligated to participate in, develop, implement, and enforce these management measures. In 2016, the International Commission for the Conservation of Atlantic Tunas (ICCAT), the regional fisheries management organization which manages bluefin tuna, implemented an electronic Bluefin tuna Catch Documentation System (eBCD) that contains information on the global trade of Atlantic bluefin tuna and whose members are mandated to use the system. All U.S. traders of Atlantic bluefin including importers, exporters, and re-exporters are required to use this one central system. The Import Monitoring Program processes tens of thousands of statistical and catch documents per annum. These documents are provided to IATC as electronic files, hard copy faxes and copies that require the data to be read, edited, and manually entered into electronic databases by Data Entry contractor(s). The Import Monitoring Program also manages the use of the electronic Bluefin tuna catch document system by U.S. traders. As part of that management, new U.S. traders will need to be given user accounts. Traders will need assistance with this program to retrieve the catch documents associated with their inbound shipments. Exporters will need assistance in creating export documents for domestically caught Atlantic Bluefin tuna, and U.S. traders will need assistance with validation of U.S. re-exports. Duties: Applicants will need to have experience: 1) viewing and entering data into web-based platforms including data entry screens, 2) using excel, 3) entering complex data from hardcopy documents accurately into electronic databases, 4) have the ability to engage with the public in a professional manner, 5) have good communication skills, 6) database management experience, and 5) be a self-starter who does not need a high degree of oversight. The Process Control Officer requirements include: 1) organize, edit, enter, and manage data from electronic files and hardcopy statistical and re-export documents received by the Trade Monitoring Program, 2) perform QA/QC review, 3) edit entered data based on input from QA/QC data reviews performed by data entry staff, 4) identify and communicate problems and efficiency issues related to the data entry process, data entry systems, and digital biweekly system to Import Monitoring Program Team Leads for corrections and modifications, 5)perform document preparations 6) Candidates for the Process Control Officer shall have at least one year of experience performing data management, data manipulation, and data entry duties on similar high throughput and time sensitive data entry contracts. The eBCD support line is open during regular business hours on weekdays and on Saturdays 9 am - 12 pm (ET). Candidates would need to be able to cover Saturday hours and adjust their hours during the regular workweek as appropriate so hours do not exceed 40 hours a week. One year of experience performing data management, data manipulation, and data entry duties on similar high throughput and time sensitive data entry contracts. Required Knowledge and Experience A high school diploma One year of experience performing data base management, data manipulation, and data entry duties on similar high throughput and time sensitive data entry contracts. Viewing and entering data into web-based platforms including data entry screens Using excel Entering complex data from hardcopy documents accurately into electronic databases Ability to engage with the public in a professional manner Good communication skills, Be a self-starter who does not need a high degree of supervison. Start Date: As soon as possible after completing a background check. Location: NOAA/NMFS/National Seafood Inspection Laboratory, 3209 Frederic Street,Pascagoula, MS 39567. Partial telework may be authorized. Salary and Benefits: This is a full-time position with benefits. Salary $22 to $24/hour.

IEH Laboratories, a Leader in Food Safety, is now accepting multiple applications for the Laboratory Analyst position at its facility in Guadalupe, CA. Ideal candidates will possess the following: • A BS or BA in the biological sciences or related field (required) • Proficiency with data entry and computer applications • Strong attention to detail • Ability to multitask and work in a fast-paced environment • Strong written and verbal communication skills • Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. The pay range for this position is $21.00 - $23.00 hourly. This is a full-time position and is eligible for the following benefits after a brief waiting period: medical, dental, vision, life/AD&D insurance, long- and short-term disability insurance, 401(k), health and dependent care FSA plans, employee assistance program, 15 days of paid time off per year for sick leave and/or vacation, 3 days paid bereavement leave, and 6 paid holidays per year. The shift for this position is Monday through Friday, from 12:00pm - 8:30pm. The laboratory operates 24/7, so candidates must be willing to work some weekends. This position requires regular on-site presence at our lab in Guadalupe, California (remote work is not available). While we welcome applications from all qualified candidates authorized to work in the United States, please note that candidates must either currently reside in the local area or be willing to relocate at their own expense, as relocation assistance is not provided. Due to exposure to various food allergens in the laboratory environment, applicants with moderate to severe food allergies are discouraged from applying. To apply for this position please access the company's job posting at: https://apps.iehlabs.com/applyatieh.html#68a905c77a656af580bcbee0 After navigating to the URL listed above, you will be asked to complete optional self-identification surveys and submit your cover letter, resume and references in a combined, single(1) PDF. Equal Opportunity Vet/Disability "Know Your Rights" Poster: https://www.eeoc.gov/sites/default/files/2022-10/EEOC_KnowYourRights_screen_reader_10_20.pdf

Trialmed Melbourne (formerly Optimal Research Melbourne) is looking for overall healthy volunteers to participate in a clinical research trial to help advance vaccine research. Qualifications: • 18 to 70 years old • Health status is further evaluated by reviewing medical history, screening assessments, and visit with physician • Available and willing to commit to the trial visit structure - You will be asked to come to our clinic for 8 outpatient visits and 2 follow-up phone calls Eligible participants will receive trial related care and assessments at no cost and may be compensated up to $1,250 for trial related time. If you are interested in participating, please complete the contact form. We will follow up with more information and schedule an appointment to see if you qualify. Additional Details

Breathe Easier: Join Our Asthma Clinical Trials! Are you or someone you care about dealing with Asthma? Take a step toward improved breathing by participating in our clinical trials aimed at discovering new treatments and enhancing Asthma care. We are seeking patient volunteers to help us evaluate the effectiveness of a new medication for Asthma. There’s no cost for the medication, and you’ll be compensated for your time and travel related to the study. Call (408) 443-5340 Now! Or Apply Here Why Participate? Compensation: Get compensated for up to $800! Comprehensive Support: Regular check-ins and assessments to ensure your health is a priority. Our trial is conducted by experienced healthcare professionals dedicated to your well-being. Study medications: Study-related medication for Asthma are given at no cost. To qualify: *Must be male or female between 21-75 years of age *Clinical Diagnosis of Asthma for 12 months *Non smokers or vapers Check out our other studies! * Chronic Low Back Pain * Type 2 Diabetes * Refractory or Unexplained Chronic Cough * Future Studies San Jose Clinical Trials Let’s work together towards better health! Call us today at (408) 443-5340 or visit https://sanjosetrials.com/ to learn more and see if you qualify.