Who We Are Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation inspiring complex change, enabling organizations to grow, building competitive advantage,

1. Oversee three to four active clinical studies; tasks include the planning, development, and implementation of clinical protocols. 2. Manage recruitment, screening, enrollment, consenting and conducting study visits of clinical research subjects. 3. Collect and enter data and manage study databases. 4. Preparation and submission of research protocol to the IRB. 5. Ensur

Under supervision, performs non invasive diagnostic tests for cardiovascular, cerebrovascular, peripheral arterial and peripheral venous diseases in order to support the goal of quality patient care. Position Vascular Laboratory Technologist Department Vascular Lab Schedule Full Time JOB REQUIREMENTS EDUCATION 2 years of technical training beyond high school CERTIFICATES,

Responsible for day to day oversight and management of assigned projects. Responsible for development and maintenance of Trial Master File (TMF), Assists PI with protocol and consent form development for initial application and with subsequent amendment changes. Initiates, plans, facilitates and oversees the research project start up, active and close out phases; for PI I

Analyze medical and surgical products to identify savings opportunities. Support cost savings initiatives by presenting data analysis to physicians, clinicians, and administrators. Provide analyses to assist with strategic decision making. Utilize third party systems, such as Healthcare IQ, Vizient tools, and Optum, to identify savings opportunities. Manage data flow and

Under the direction of the Director of Automation, the Senior Manager, Sicence Automation plans, organizes schedules and directs the work of the Automation group in the Molecular Genetics and Oncology department. Also, has the responsibility for the management of automation projects. Ensures that goals and objectives of the project(s) are accomplished within prescribed ti

Home Based, US As a Sr Quality Manager in Technology Quality Management (TQM) you will manage efforts to define, adopt and oversee compliance to processes and standards as the fundamental baseline for technology solution development, validation and delivery. You will support efforts, in collaboration with the business to monitor, identify and implement continuous process

Aids with research studies as per guidelines and protocols. Approaches patients to fill out surveys and ensures completion. Follows up with patients to ensure questionnaires are completed. Working within existing data systems to ensure correct tabulation of data. Organizes and processes study data. Creates and maintains databases/files containing study data using standard

Primary responsibility will include management and maintenance of clinical and research databases and assistance with chart and database abstraction. Recruitment and consent of patients for enrollment on research studies Oversight of the research study start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activati

Reserved for Pre selected Candidate Perform original research. Mentor research trainees. Participate in teaching of graduate students as appropriate. Serve on committees at the Mass Eye and Ear and Harvard Medical School. Qualifications Ph.D. EEO Statement Massachusetts Eye and Ear is proud to be an equal opportunity employer and is committed to providing a workplace free

1. Provides assistance on clinical research studies as per study guidelines and protocols. 2. Recruits and evaluates potential study patients. Per protocol instruction, conducts telephone interviews or schedules patient for study visit and screening. May be required to perform clinical tests such as phlebotomy, EKGs, etc. 3. Interact with patients/subjects with regard to

Reporting to the Director of Biosafety, the Associate Biosafety Officer maintains the integrity of the DFCI Biosafety and Import/Export Controls Compliance Programs and support for the DFCI research program and pharmacy USP797 sterile compounding program. This includes being the administrator for the Institutional Biosafety Committee (IBC), the overall Biosafety and Biose

Principal Astronomer Job Location US MA Cambridge Requisition ID 2022 6210 Overview Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical e

General Summary of Position The essential purpose of this position is to supplement the PI's technical expertise in neurophysiology and create a strong scientific and professional management team for training and educating undergraduate and graduate researchers in biomedical engineering. Minimum Qualifications (Required) Education PhD or MD Experience 3+ years conducting

of Position Research Scientist Position at the CME Group of the Space Science Center at the University of New Hampshire. Acceptable minimum level of education Doctorate Acceptable minimum years of experience None Additional Job Information Posting Number PS4612FY24 Other minimum qualifications 3 peer reviewed manuscripts accepted and/or published. Experience working with i