Scientist - Clinical Research jobs in Orland Park, IL

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.
  • 7 Days Ago

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Clinical Research Associate
  • Advanced Clinical
  • Chicago, IL FULL_TIME
  • OVERVIEWWe are currently searching for a skilled professional to join a well-known client's team as a remote Clinical Research Associate. The CRA is responsible for the management of day-to-day aspect...
  • 2 Days Ago

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Clinical Research Coordinator
  • Revival Research Institute, LLC
  • ELGIN, IL FULL_TIME
  • Unique opportunity to make an Impact in the healthcare industry… Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since...
  • Just Posted

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Clinical Research Coordinator (CRC)
  • Center for Clinical and Translational Science
  • Chicago, IL FULL_TIME
  • Clinical Research Coordinator, UIC Center for Clinical and Translational ScienceThe Clinical Research Coordinator works within the CCTS Clinical Research Center and is responsible for managing and coo...
  • 19 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...
  • 1 Month Ago

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Senior Clinical Research Associate (West Coast - Oncology)
  • Advanced Clinical
  • Deerfield, IL FULL_TIME
  • ***This position can work remotely anywhere in the United States*** What's in it for YOU? Competitive compensation with comprehensive medical, vision, and dental benefits package 10 paid holidays incl...
  • 1 Month Ago

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0 Scientist - Clinical Research jobs found in Orland Park, IL area

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Environmental Scientist
  • Eps Environmental Services
  • Chicago, IL
  • Company Description EPS Environmental Services is an environmental consulting firm headquartered in Chicago, IL. We spec...
  • 4/30/2024 12:00:00 AM

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Senior Scientist
  • Bausch + Lomb
  • Westchester, IL
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/29/2024 12:00:00 AM

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Nurse Scientist
  • Rush University
  • Chicago, IL
  • Job DescriptionLocation:Chicago, ILHospital:RUSH University Medical CenterDepartment:Dept Of Professional NursPractWork ...
  • 4/29/2024 12:00:00 AM

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Data Scientist
  • hackajob
  • Chicago, IL
  • Exciting Opportunity Alert! hackajob has partnered with a Leading Airline for this Data Scientist role. Are you passiona...
  • 4/28/2024 12:00:00 AM

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Environmental Scientist
  • Eps Environmental Services
  • Chicago, IL
  • Company Description EPS Environmental Services is an environmental consulting firm headquartered in Chicago, IL. We spec...
  • 4/28/2024 12:00:00 AM

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Beverage Scientist
  • Hirewell
  • Niles, IL
  • Scientist - Product Development Summary of Position The Scientist role within the Product Development team is primarily ...
  • 4/28/2024 12:00:00 AM

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Data Scientist
  • Caterpillar Financial Services Corporation
  • Chicago, IL
  • Career Area:Business Technologies, Digital and Data Job Description:Your Work Shapes the World at Caterpillar Inc.When y...
  • 4/28/2024 12:00:00 AM

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Staff Scientist
  • Loyola University Chicago
  • Maywood, IL
  • Job Description Job Description A Staff Scientist position is available in the laboratory of Drs. Elliot and Glassberg t...
  • 4/26/2024 12:00:00 AM

Orland Park is a village in Cook County, Illinois, United States, a suburb of Chicago, which in 2010 had a population of 56,767. 25 miles (40 km) southwest of Chicago, Orland Park is close to several interstate highways, with the I-80 east-west coast connector as its southern border. The Metra commuter rail system links it to the Chicago Loop and from there to O'Hare and Midway airports. According to the 2015 census, Orland Park has a total area of 22.167 square miles (57.41 km2), of which 21.88 square miles (56.67 km2) (or 98.71%) is land and 0.287 square miles (0.74 km2) (or 1.29%) is water....
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Scientist - Clinical Research jobs
$85,459 to $121,509
Orland Park, Illinois area prices
were up 0.8% from a year ago

Scientist - Clinical Research in El Paso, TX
DDCF's Medical Research Program created the Clinical Scientist Development Award to provide mentored research funding to early-career physician-scientist faculty to enable their transition to independent and successful research careers.
December 01, 2019
Scientist - Clinical Research in Green Bay, WI
Jude Children’s Research Hospital, talented faculty and staff work together and with colleagues worldwide-to advance the resear.
January 26, 2020
Scientist - Clinical Research in Sacramento, CA
Bachelor s in Life Sciences or related field with 2 plus years of clinical research experience.
January 11, 2020