Researcher Salary at Carolina Blood BETA

Senior Data Scientist, Search and Lookup Services, FactSet Research Systems Inc. Jersey City, NJ: Works alongside both the product and engineering teams to build and optimize search algorithms as well as provide insights that enable data-driven decision making. Provide technical input to high-impact team, develop practices in a production environment; and taking data analysis to influence change in either business functions or products while using critical skills. This will include the development and understanding of Product lifecycle at FactSet and identify areas where data-driven insights that can increase the efficiency and effectiveness of business decisions. Complement key product initiatives with Data Science techniques to ensure Product decisions are supported by the underlying usage data by challenging assumptions, proposing data discovery actions to affirm assumptions, and evaluate post-release usage to assess the effectiveness of product changes. Identify and develop user me

Director, GLP Quality Assurance & Compliance Shape the Future of Quality & Compliance in Preclinical Research Are you a seasoned GLP Quality Leader looking to build something from the ground up? Join a pioneering in vivo research organization at the forefront of translational medicine, where your expertise in GLP compliance and quality assurance will drive excellence in preclinical studies. We are seeking a Director, GLP Quality Assurance & Compliance to establish and lead our Quality Assurance Unit (QAU) and ensure full compliance with regulatory standards. Why Join Us? Be part of a cutting-edge research facility dedicated to advancing preclinical science. Lead the development of a GLP-compliant QAU from a fresh, bare facility to full compliance. Work on Surgical, PK, Cardiovascular, Bioanalysis, Anatomic Pathology, and Histology studies. Implement and transition from a paper-based QA system to Pristima or Provantis. Play a critical role in AALAC inspections and ensure compliance with

Job Summary: To identify needs for (through auditing or other methods)and provide coding education related to HCC (Hierarchical Category Coding). Serve as a liaison to ambulatory Clinical Documentation Specialists regarding coding guidelines and documentation required to capture HCCs for Risk Adjustment coding. Train and educate coding staff on HCC coding issues. Work with payer representatives who audit HCC coding for Managed Medicare plans and participate in the sharing of those audits with staff and other departments as needed. Develop new procedures related to HCC coding and assist with implementation of systems that impact coding, such as 3Ms Ambulatory Module Research payer guidelines or regulatory guidelines that impact coding (ICD10 or CPT) and provide education for Ambulatory Coding Department related to those issues, understanding of claim edits, and denials by payers for coding reasons, to help prevent future denials. Promotes teamwork and act as a liaison with coders and ot

Job Description Job Description We at Carolina Blood and Cancer Care Associates are in search of an organized professional who can join our Clinical Trials Team. The Research Coordinator works directly with Trial Sponsors, CRAs, and other Medical staff. A clinical research coordinator will work on studies designed to measure the effectiveness of a drug, medical device, or process on the human body. You will interact directly with patients by screening them as potential candidates, collecting data and entering data for the study. Work responsibilities can include coordinating a clinical research study by identifying patients, tracking inventory, interacting with patients, collecting data, and overseeing protocols. Basic understanding of Medical terminology and Clinical Research. Needs to be a fast learner. Tech savvy and good data entry skills. Need to be organized and have the ability to communicate effectively.

Job Description Job Description Director of Clinical Development – Charlotte Metro/SC - #8175 The Director of Clinical Development will provide scientific support across Veterinary Sciences, Research and Development and Commercial programs. This position works with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution and ensure Good Clinical Practices (GCPs) are followed. The incumbent will help develop protocols, review trial data, interact with external stakeholders and participate and contribute scientific expertise for ongoing clinical trials focusing on body systems except the Musculoskeletal system. Responsibilities: Direct and plan clinical research and develop timetables, budgets and resource analysis for clinical research and personnel administration. Participate in due diligence activities for potential business development opportunities from a research perspective. Design, implement and monitor clinical research to ensure timely com

We are seeking a BC/BE Family Practice Provider for a 100% outpatient opportunity just outside Charlotte, North Carolina. Enjoy both worlds-a peaceful, rural community with easy access to the urban amenities in Charlotte and Winston-Salem. Excellent schools, affordable housing, a mild climate, and a diverse business community add to the appeal of this peaceful community. Practice details include: Hospital Employee, Outpatient only M-F, no weekends No Call Competitive Annual Salary Quality Bonus production incentives Loan Forgiveness possible Signing Bonus possible, contact us for details Relocation Bonus available CME up to 1 week and money available Ancillary income possible 401K A great community for family and an abundance of friendly, southern warmth Excellent schools, affordable housing, a mild climate, and a diverse business community An easy drive to Charlotte and Winston-Salem Reimbursement for required licenses, DEA and associated fees 100% outpatient with No call, No night an

Job Description Job Description Monroe Biomedical Research is preparing for significant expansion of its clinical research operations, including expanded infrastructure and new clinical trial site locations. We are looking for an ambitious Clinical Research Coordinator to join our team! As a Clinical Research Coordinator, you will play a crucial role in clinical research activities, on-site in Monroe, North Carolina. The CRC will interact directly with patients and MBR staff alike, will perform study procedures, and will collect, manage, and submit study data. The right incumbent for the role must therefore be meticulous, organized and diligent. While MBR will provide support and training, Clinical Research Coordinators are expected to work independently and take full ownership/responsibility of their assigned clinical trial. Key Responsibilities: · Designing and maintaining source documentation/workflows based on study protocol requirements · Organizing study patient visits · Performi

Job Title: Event Planner Location: Charlotte, NC Job Summary and Description: The Event Planner collaborates with EPRI event hosts to plan and execute multiple types of events of varying complexity to ensure a successful business outcome. The Event Planner provides expert consultation across the institute in an effort to drive consistent application of EPRI event protocol, branding and a successful event experience. The event planner exudes strong time management, project management and customer-focused communication to ensure clear and positive ROI for all EPRI Events. Key Responsibilities: •Responsible for collaboration, proactive engagement and end-to-end event management for events hosted by assigned key stakeholders and other event hosts, as assigned. •Serve as the principal liaison between event host and suppliers throughout the planning and execution process •Cultivate and maintain effective relationships internally with key stakeholders, internal departments and vendors to ensu