Researcher Salary at Mpcr Lab BETA

The Clinical Research Project Manager position is an excellent opportunity for an individual who is interested in assisting a fast-emerging biopharmaceutical company conduct unique first-in-human, clinical research trials with multiple therapeutics. You will work under general supervision to manager a number of clinical research studies and manages data collection and submissions for multiple clinical trials. This position entails a high volume of document control and data abstraction; no patient contact. Principal Duties And Responsibilities The following duties will be performed under general supervision by the VP of Research and Manufacturing: · Manage several ongoing and future clinical research project · Write clinical research protocols · Monitor and evaluate protocol compliance · Manage data collection via chart abstraction and submit data · Write informed consent documents · Monitor and report adverse events as required by institutional/federal regulations · Prepare submission

Position Summary: This position will be responsible for the development of new roofing and waterproofing products for residential and commercial applications. He/She will be responsible for development of new products, improvement of existing products, advance laboratory testing, competitive analysis as well as value engineering initiatives intended for existing product lines. Position reports directly to the Principal Scientist or Manager of R&D and may supervise other scientists and research technicians. Responsibilities: Work independently, manage research projects and work in teams towards executing the initiatives of the Manager of R&D and the research team Generate ideas that will enhance existing products and lead to the development of new products, test procedures and protocols. Develop investigative work resolving associated technical issues on products and projects Use sound scientific principles such as statistical analysis, material science, rheology and solid mechanics. Cr

We are looking to add a Site Manager to our growing team. This person would be responsible for overseeing 2 sites focused on Medical Device and Therapeutic clinical trials. This is a full time onsite role with lots of room for growth, fantastic benefits and the opportunity to join a large national organization that is changing the future of therapeutics. Job Description A Site Manager in clinical research plays a crucial role in overseeing and managing clinical trial sites within a specific geographic area. Their responsibility spans from site selection to ensuring that clinical studies are conducted in compliance with regulatory standards and study protocols. Responsibilities: Oversee and monitor the day-to-day operations of clinical trial sites in the region. Ensure that the sites adhere to protocol requirements, Good Clinical Practice (GCP), and regulatory guidelines. Provide support to sites during the initiation, monitoring, and close-out phases of the trial. Track and assess site

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary: Provides direct support t

ASR Group is the world's largest refiner and marketer of cane sugar, with an annual production capacity of more than 6 million tons of sugar. The company produces a full line of grocery, industrial, food service and specialty sweetener products. Across North America, ASR Group owns and operates six sugar refineries, located in Louisiana, New York, California, Maryland, Canada and Mexico. In Europe, the company owns and operates sugar refineries in England and Portugal. ASR Group also owns and operates mills in Mexico and Belize. The company's brand portfolio includes the leading brands Domino®, C&H®, Redpath®, Tate & Lyle®, Lyle's® and Sidul®. OVERVIEW The NPD Research Scientist II will be a leader on new product innovation and successfully develop and execute projects within the organization. Initial area of focus will include product development for the Tellus molded fiber business. The individual will independently research, design, conduct experiments, gather data, develop prelimin

HIGHLIGHTS Full-time opportunity with consistent weekday schedule (Monday–Friday, 7:00 AM – 3:30 PM) Comprehensive benefits including health insurance, PTO, and 401k match Join a thriving research network with long-term growth potential Hands-on work supporting impactful clinical trials across multiple phases Collaborative, inclusive, and mission-driven culture COMPANY Our client is one of the fastest-growing site networks in the country, with 31 locations across 9 states—and they’re not slowing down. With a strong focus on career development, diversity, and advancing medical research, this organization offers a unique opportunity to grow your career while contributing to meaningful, life-changing work. POSITION We’re seeking a Clinical Research Coordinator to join our client’s Boca Raton, FL team. In this role, you’ll assist with the execution of clinical trials across various phases and therapeutic areas. You’ll work closely with patients, investigators, and sponsors to ensure protoc

Who You Are A highly analytical thinker with strong financial modeling and research skills Able to synthesize complex data into clear, actionable investment insights A proactive, detail-oriented professional with strong communication and presentation abilities You enjoy building authentic working relationships with team members and external stakeholders You are flexible, think creatively, and demonstrate a positive and solution-oriented demeanor in the face of complexity Passionate about private credit, technology investments, and working directly with company leadership About the Team Serengeti Asset Management is an opportunistic, value-driven investment firm that provides flexible capital solutions for innovative private companies and their shareholders. We invest in and build financing platforms for assets often ignored or underserved by other, more traditional capital sources. Our capital solutions seek to address complex situations through structure and creativity. Your role will

Highlights Full time clinical research opportunity - focus on just cardiology research! M-F or 4 day work week options, no weekends, lots of stability and work life balance! Have a large impact working with a growing organization , opportunities for fast advancement! Work on sponsor backed trials at the site level! Relocation assistance provided if needed! The Role The Cardiologist Principal Investigator is responsible for oversight and execution of clinical trials that test new medications on the behalf of sponsor/pharmaceutical companies! You will work in a clinic to promote Good Clinical Practice and follow research protocols assigned. This includes things like medical management of patients on trial, administering medications, documentation, tracking and management of adverse events, and overall management of the study. You will have a team of skilled coordinators, NPs, and assistants as well! Evaluate and screen potential subjects based on study eligibility criteria Perform and re