Scientist - Clinical Research jobs in Illinois

Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)

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Clinical Research Coordinator III
  • DM Clinical Research
  • Chicago, IL FULL_TIME
  • Clinical Research Coordinator III

    A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.


    DUTIES & RESPONSIBILITIES
    • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
    • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
    • Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
    • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
    • Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
    • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
    • Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
    • Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
    • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
    • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
    • Ability to train and mentor site staff, as needed
    • Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
    • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
    • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
    • Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
    • Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
    • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
    • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
    • Being prepared for and available at all required company meetings.
    • Submitting required administrative paperwork per company timelines.
    • Occasionally attending out-of-town Investigator Meetings
    • Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
    • Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
    • Facilitate effective communication between patients, healthcare providers, and research staff
    • Any other matters as assigned by management

    KNOWLEDGE & EXPERIENCE

    Education:
    • High School Diploma or equivalent required
    • Bachelor's degree preferred
    • Foreign Medical Graduates preferred
    Experience:
    • Minimum of 5 years experience in Clinical Research
    • Supervisory experience preferred
    • Wide therapeutic range of clinical trials experience preferred
    • Regulatory research experience is a plus
    Credentials:
    • ACRP or equivalent certification is preferred
    Knowledge and Skills:
    • Goals-driven while continuously maintaining quality.
    • Must be detailed-oriented, proactive, and able to take initiative.
    • Must have strong written and communication skills.
    • Must have excellent customer service skills.
    • Proficient communication and comprehension skills both verbal and written in the English language are required.
    • Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
  • 2 Months Ago

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Research Scientist I - Materials Discovery Research Institute
  • UL Research Institutes
  • Skokie, IL FULL_TIME
  • Job DescriptionAt UL, we know why we come to work.We have an exciting opportunity for a Research Scientist I/Lab Technician at UL Research Institutes Materials Discovery Research Institute, based in o...
  • 10 Days Ago

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Research Scientist II - Materials Discovery Research Institute
  • UL Research Institutes
  • Skokie, IL FULL_TIME
  • Job DescriptionThe Materials Discovery Research Institute (MDRI), a division of Underwriters Laboratories Research Institutes (ULRI), is currently seeking a Research Scientist II. In this role, you wi...
  • 10 Days Ago

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Research Plant Physiologist/Physical Scientist (Research Associate)
  • US Agricultural Research Service
  • Urbana, IL FULL_TIME
  • Duties Increase the efficiency and productivity of photosynthesis, growth, and yield of crop plants, especially in the context of global climate change and environmental uncertainty. Develop a basic m...
  • 1 Day Ago

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Clinical Research Physician
  • GenHarp Clinical Solutions
  • Evergreen, IL FULL_TIME
  • The Clinical Research Physician (Principal Investigator) role will be based in Evergreen Park, IL, and is a part-time contract position. This role is hybrid (remote and on-site). Job Duties & Responsi...
  • 11 Days Ago

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Senior Clinical Research Associate
  • OnPoint Clinical Staffing Services
  • Chicago, IL FULL_TIME
  • Job DescriptionSenior CRAResponsibilities include:* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical t...
  • 21 Days Ago

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Senior Scientist
  • Meet
  • Ridgefield, CT
  • Our esteemed client, a leading top 20 pharmaceutical company known for its continuous growth, is seeking a Senior Scient...
  • 6/12/2024 12:00:00 AM

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Process Development, Senior Scientific Specialist (Contract)
  • Vertex Pharmaceuticals
  • Boston, MA
  • Job Description: General Summary: Vertex is looking for a talented individual to join our team as a scientific specialis...
  • 6/12/2024 12:00:00 AM

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Associate Scientist / Scientist
  • SystImmune
  • Redmond, WA
  • Company Overview: SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. O...
  • 6/12/2024 12:00:00 AM

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Principal Scientist, Clinical Research
  • J&J Family of Companies
  • Cincinnati, OH
  • Principal Scientist, Clinical Research - 2406190642W **Description** Johnson & Johnson, we believe health is everything....
  • 6/10/2024 12:00:00 AM

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FEMA - Scientific Specialist (Nationwide Openings)
  • Idaho State Job Bank
  • Nampa, ID
  • FEMA - Scientific Specialist (Nationwide Openings) at CDM Smith in Nampa, Idaho, United States Job Description 27234BR R...
  • 6/9/2024 12:00:00 AM

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FEMA - Scientific Specialist (Nationwide Openings)
  • Idaho State Job Bank
  • Idaho Falls, ID
  • FEMA - Scientific Specialist (Nationwide Openings) at CDM Smith in Idaho Falls, Idaho, United States Job Description 272...
  • 6/9/2024 12:00:00 AM

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Principal Scientist, Clinical Research, Breast Cancer
  • Merck
  • Rahway, NJ
  • **Job Description** Our company is a global health care leader with a diversified portfolio of prescription medicines, v...
  • 6/8/2024 12:00:00 AM

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Associate Scientist / Scientist
  • Meet
  • Thousand Oaks, CA
  • I am partnered with an exciting Biotech company out of Thousand Oaks, CA looking to grow their team with an Associate Sc...
  • 6/8/2024 12:00:00 AM

Illinois (/ˌɪlɪˈnɔɪ/ (listen) IL-ih-NOY) is a state in the Midwestern and Great Lakes region of the United States. It has the fifth largest gross domestic product (GDP), the sixth largest population, and the 25th largest land area of all U.S. states. Illinois is often noted as a microcosm of the entire United States. With Chicago in northeastern Illinois, small industrial cities and immense agricultural productivity in the north and center of the state, and natural resources such as coal, timber, and petroleum in the south, Illinois has a diverse economic base, and is a major transportation hu...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Scientist - Clinical Research jobs
$85,850 to $122,061

Scientist - Clinical Research in Savannah, GA
Most scientists choose to complete a dual degree, in both science and medicine.
January 10, 2020
Scientist - Clinical Research in Fort Wayne, IN
Natural sciences managers supervise the work of scientists, including chemists, physicists, and biologists.
February 15, 2020
Scientist - Clinical Research in Norwich, CT
Research projects may be aimed at improving manufacturing processes, advancing basic scientific knowledge, or developing new products.
December 15, 2019