Scientist - Clinical Research jobs in Elizabeth, NJ

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
  • Jersey, NJ 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.
  • 1 Day Ago

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Clinical Research Scientist
  • Global Channel Management, Inc.
  • Madison, NJ FULL_TIME
  • Company DescriptionGlobal Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of e...
  • 1 Month Ago

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Clinical Research Scientist
  • Mitsubishi Tanabe Pharma America
  • Jersey, NJ FULL_TIME
  • Company DescriptionEntrepreneurialSpirit, Rooted in Tradition. At Mitsubishi Tanabe Pharma Development America (MTDA), we can tout a storied reputation more than 300 years in the making. Our parent co...
  • 1 Month Ago

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CRC III
  • DM Clinical Research
  • Jersey, NJ FULL_TIME
  • Clinical Research Coordinator III The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regu...
  • 1 Month Ago

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Research Scientist (NBOE)
  • Newark Public Schools
  • Newark, NJ OTHER
  • Position Type: Non Instructional - All Titles/Research ScientistDate Posted: 8/30/2023Location: Research Eval. & Testing - 432NEWARK BOARD OF EDUCATION HUMAN RESOURCE SERVICES 765 BROAD STREET, NEWARK...
  • 15 Days Ago

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Clinical - Pharmacovigilance (PV) Scientist
  • TechDigital Corporation
  • Madison, NJ FULL_TIME
  • Position is Onsite Functional Area Description The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The Worldwide Patient Safety group is responsible for pharmac...
  • 3 Days Ago

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0 Scientist - Clinical Research jobs found in Elizabeth, NJ area

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Senior Scientist
  • Bausch + Lomb
  • Elizabeth, NJ
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/24/2024 12:00:00 AM

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Senior Principal Scientist, Clinical Research, Hematology/Lymphoma
  • Merck & Co., Inc.
  • Rahway, NJ
  • Job Description Our company is a global health care leader with a diversified portfolio of prescription medicines, vacci...
  • 4/22/2024 12:00:00 AM

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Scientist
  • Indotronix Avani Group
  • Franklin Lakes, NJ
  • Job Title: Scientist Chemistry II Location: Franklin Lakes NJ 07417 (Hybrid 3 days per week onsite) Duration: 12 months ...
  • 4/22/2024 12:00:00 AM

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Scientist/Engineer
  • Yoh, A Day & Zimmermann Company
  • Summit, NJ
  • Job Description Job Description Scientist/Engineer - Summit, NJ 12 month contract W2 Pay rate: $48.94/hr The Scientist/E...
  • 4/22/2024 12:00:00 AM

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Principal Scientist, Clinical Research, Breast Cancer
  • Merck & Co., Inc.
  • Rahway, NJ
  • Job Description Our company is a global health care leader with a diversified portfolio of prescription medicines, vacci...
  • 4/21/2024 12:00:00 AM

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Principal Scientist
  • Bausch + Lomb
  • Elizabeth, NJ
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/21/2024 12:00:00 AM

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Scientist
  • Indotronix Avani Group
  • Franklin Lakes, NJ
  • Job Title: Scientist Chemistry II Location: Franklin Lakes NJ 07417 (Hybrid – 3 days per week onsite) Duration: 12 month...
  • 4/20/2024 12:00:00 AM

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Senior Scientist
  • Bausch + Lomb
  • Elizabeth, NJ
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/20/2024 12:00:00 AM

Elizabeth is both the largest city and the county seat of Union County, in New Jersey, United States.[21] As of the 2010 United States Census, the city had a total population of 124,969, retaining its ranking as New Jersey's fourth most populous city, behind Paterson. [22] The population increased by 4,401 (3.7%) from the 120,568 counted in the 2000 Census, which had in turn increased by 10,566 (+9.6%) from the 110,002 counted in the 1990 Census.[23] For 2017, the Census Bureau's Population Estimates Program calculated a population of 130,215, an increase of 4.2% from the 2010 enumeration, ran...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Scientist - Clinical Research jobs
$94,349 to $134,143
Elizabeth, New Jersey area prices
were up 1.6% from a year ago

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Bachelor s in Life Sciences or related field with 2 plus years of clinical research experience.
January 11, 2020