Clinical Data Coordinator Salary at Wheaton Franciscan Services Inc BETA

You're eager to lead innovative projects and make a big impact in medical research. In a dynamic leadership role, you will oversee the Registry Analytics Institute (RAI) for the AAOS Program of Registries, where you'll guide and manage the RAI, pushing our mission and vision forward. You'll oversee and develop the International Prosthesis Library (IPL), and kickstart and manage relationships and projects related to grant-funded research. As a key liaison for registry subcommittees focused on research and publications, you'll provide valuable input to data specifications and act as a second-tier escalation point for registry outcome issues. You bring strong leadership, innovative thinking, great communication skills, a collaborative nature, incredible analytical skills, project management expertise, problem-solving abilities, and a passion for advancing medical research and improving patient outcomes. If this sounds like you, please read on! The Research Director will be responsible for

Location: Chicago, IL Hospital: Rush University Medical Center Department: Rush Alzheimers Dis Ctr-ResFac Work Type: Full Time (Total FTE between 0.9 and 1.0) Shift: Shift 1 Work Schedule: 8 Hr (8:00:00 AM - 4:30:00 PM) Rush offers exceptional rewards and benefits learn more at our Rush benefits page. Summary: The Lab Research Technician 2 assists basic science and/or clinical (biological) scientists to conduct routine laboratory tests and experiments. The Lab Research Technician 2 is responsible for performing scientific tests, experiments, and analyses while working under direction of a Principal Investigator (PI) and more senior lab staff. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures. Other information: Required Job Qualifications: •Bachelor's degree in biology, chemistry, or related science. •1 year of laboratory experience. •Familiarity with traditional laboratory instruments and basic knowledge of basic experimental desi

About the job Medical Laboratory Administrative Assistant Our client is looking for a dynamic laboratory administrative assistant to accurately and efficiently assist clinical operations. A successful candidate will be highly organized and possess an excellent, can-do attitude. This position will report directly to the laboratory director, ensuring the lab director knows what tasks are awaiting his/her input, contacting clients on the director's behalf, filing and scanning paperwork, performing some data entry, answering phones as needed and providing general administrative support to the laboratory management. The candidate must be flexible, and be able to successfully manage multiple work streams at the same time. Administrative / Customer Service Responsibilities Organize lab documents and paperwork, including filing and data entry Answer phones and provide customer support as needed Contact clients with information requests, relaying information, clarifying details; resolve and esc

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **ABOUT ABBOTT DIAGNOSTICS** The key to successful treatment and full recovery is often fast, accurate diagnosis. Abbotts life-changing tests and diagnostic tools provide insights that enable smarter, faster decisions and transform the way the world is managing health. Our pioneering technology spans the world of healthcare operations with medical diagnostic instruments, tests, automation and informatics solutions for hospitals, reference labs, blood centers, emergency departments, physician offices and clinics. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self

Department: MED-Clinical Trials Unit Salary/Grade: NEX/11 Target hiring range for this position will be between $19.31-$24.14 per hour. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data. Job Summary: Coordinates collection, analysis, processing & reporting of data & assists Principal Investigator (PI) in judging the validity of test data obtained in regard to biomedical &/or social-behavioral research study(ies) of limited complexity involving co-investigators, multiple campuses &/or universities. Completes all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). On site activity is required 3-

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities).

Opportunity to join the Quality Department of one of the fast-growing clinical research companies! This is an excellent opportunity for clinical research professionals to get into data and quality! Ideal backgrounds would include experience working in healthcare quality, regulatory, or patient data. Clinical research experience is not required but is nice to have. If you are a Clinical Research Assistant or Coordinator looking to get into Data and Quality, please consider applying as well. HIGHLIGHTS Play a major role in helping patients get involved in cutting-edge clinical trials - a meaningful healthcare position! Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days of PTO, 10 Paid Holidays) Gain experience in the fast-growing world of clinical research and develop skills that are in high demand Monday - Friday 8:30 am - 5 pm The company is invested in growth, providing employees with unique opportunities for career advancement POSITION The Quality Control Data Managemen

Location: Chicago, IL Hospital: RUSH University Medical Center Department: Int Med Infect Disease-Res Fac Work Type: Part Time (Total FTE between 0.5 and 0.89) Shift: Shift 1 Work Schedule: 4 Hr (8:30:00 AM - 1:00:00 PM) Summary: Under minimal supervision of basic science (biological) / clinical scientists or laboratory supervisor, processes samples and conducts both specialized and complex laboratory tests, procedures and experiments in accordance with study protocols. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures. Other information: Required Job Qualifications: * Bachelor's degree with 3 years of laboratory experience. * Knowledge of both basic and specialized laboratory instruments and software programs. * Advanced knowledge of standard experimental design. * Proficient knowledge of best practice laboratory practice and principles including their application. * Attention to detail and accuracy. * Strong oral and written comm