Investigational Weight Management Study (Norman)

AMR Knoxville is conducting an investigational Type 2 Diabetes trial for participants ages 18 to 75. Qualified participants: Must have Type 2 Diabetes Must have a BMI of 27 or greater Must have been on a stable GLP-1 dose for at least 6 months Must have an A1c value of ≥7% and ≤10% managed with diet and exercise or with a stable dose of metformin and/or SGLT2 inhibitors and/or DDP4 inhibitors Cannot be using insulin Meet other study criteria Qualified participants will receive all study-related care at no cost. Reimbursement is available up to $2,250.00 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 865-305-3784 or visit their website at amrknoxville.com for more detailed information.

AMR Clinical is now enrolling in a heart failure prevention clinical research study for adults ages 40 and older who have Type 2 Diabetes and a history of heart or blood vessel disease. Qualified participants must: Have a diagnosis of Type 2 Diabetes and are on treatment Have an established cardiovascular disease such as ischemic heart disease, stroke, or peripheral arterial disease Must meet other study criteria Qualified participants will receive all study-related care at no cost. Subjects may receive up to $1,800 for study-related time and travel. If you're interested in learning more about this trial, you can reach out to AMR Clinical today by calling (251) 901-2127 or visiting their website at amrmobile.com for more detailed information.

AMR Clinical is seeking participants 18 or older who are obese or overweight for a weight loss study. Qualified participants must: have a BMI of 30 or higher or have a BMI 27 or higher with one medical condition such as high blood pressure, high cholesterol, sleep apnea, or heart disease. you must not have Type 2 diabetes. must meet other study criteria. All study-related care and investigational medication provided at no cost. Compensation is available up to $7,700.00 for study-related time and travel. Call AMR Clinical today at (251) 901-2127 or visit amrmobile.com to learn more about this trial.

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.