Clinical Research Coordinator jobs in Somerset, NJ

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)

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Clinical Data Manager
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

    Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.

    Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

    Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

    To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Clinical Data Managers for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.

    Key Accountabilities:

    • Plan, manage, control, and perform data processing and management activities for assigned projects. These tasks are performed in a timely and accurate manner and in compliance with trial Sponsors’ requirements.
    • Lead assigned data processing and management projects by applying project management skills, data processing, and management techniques. Manage timelines and coordinate activities for assigned projects.
    • Specify database validation checks for assigned studies. Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules.
    • Define and monitor clinical trial dataflow and quality control (QC) processes in accordance to corporate Standard Operating Procedures (SOPs), Good Working Practices, and unit guidelines. Perform clinical trial site monitors’ training on dataflow and QC processes.
    • Design and review patient Case Report Forms (CRFs) and database schema. Test data capture/entry screens.
    • Accurately and efficiently validate electronically captured data. Write clear queries on missing data and data points failing pre-defined range checks and/or logical checks. Lead efforts in building a standard query library for common database modules, as well as for therapeutic/drug area specific modules.
    • Perform QC procedures on assigned database during the trial and additional database closure checks at the end of the study.
    • Train and supervise Data Entry personnel and junior data management personnel on study procedures, study specific handling, and management of trial data.
    • Validate and distribute study progress status reports to internal and external study team members.
    • Assist in resolving data coding discrepancies resulting from the coding of medical events, treatment procedures, and medications.
    • Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving clinical trial data and study documentation.
    • Cooperate with and assist, when required, data management quality assurance (QA) personnel in performing QA procedures on trial CRFs, database schema, and databases for assigned studies.

    Qualifications and Experience:

    • A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data capture and management, or a Master’s or Ph.D degree in these fields with at least 1 year relevant experience.
    • In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards.
    • Strong leadership in clinical data management activities and a desire to excel in leading data management projects.

    To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.ecrscorp.com

    We thank all interested applicants, however, only those selected for an interview will be contacted.

    Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.

    #LI-Remote
    #LI-KD1


    Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

    The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)

  • 8 Days Ago

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Contracts Associate
  • Everest Clinical Research USA
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
  • 11 Days Ago

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Principal Statistical Programmer
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
  • 12 Days Ago

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Principal Biostatistician (Remote)
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
  • 12 Days Ago

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Biostatistician
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
  • 13 Days Ago

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Associate Director, Biostatistics
  • Everest Clinical Research
  • Bridgewater, NJ FULL_TIME
  • Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
  • 13 Days Ago

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0 Clinical Research Coordinator jobs found in Somerset, NJ area

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Clinical Research Coordinator
  • Emerson Clinical Research Institute
  • Passaic, NJ
  • Job Description Job Description Our clinical research company is looking to hire a qualified candidate for the full-time...
  • 3/17/2024 12:00:00 AM

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Clinical Research Coordinator - Pulmonary
  • Mount Sinai Hospital
  • New York, NY
  • Job Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and ...
  • 3/17/2024 12:00:00 AM

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Clinical Research Coordinator
  • The Institute for Family Health
  • New York, NY
  • SUMMARY Work with research team to recruit patients, manage data, and contribute to the success of innovative studies ...
  • 3/16/2024 12:00:00 AM

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Clinical Research Coordinator
  • Rutgers University
  • New Brunswick, NJ
  • Position Details Position Information Recruitment/Posting Title Clinical Research Coordinator Job Category Staff & Execu...
  • 3/15/2024 12:00:00 AM

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Clinical Research Coordinator
  • The Institute for Family Health
  • New York, NY
  • SUMMARY Work with research team to recruit patients, manage data, and contribute to the success of innovative studies to...
  • 3/15/2024 12:00:00 AM

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Jr. Clinical Research Coordinator
  • SGS Group
  • Union, NJ
  • Company Description We are SGS - the world's leading testing, inspection and certification company. We are recognized as...
  • 3/15/2024 12:00:00 AM

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Clinical Research Coordinator
  • Northwell Health
  • New York, NY
  • Job Description Job Description Coordinates and monitors research trials; actively oversees the recruitment of study par...
  • 3/14/2024 12:00:00 AM

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Bilingual Clinical Research Coordinator
  • ObjectiveHealth
  • Florham Park, NJ
  • Clinical Research Coordinator (Bilingual - Spanish) Our clinical research company is looking to hire a qualified candida...
  • 3/14/2024 12:00:00 AM

Somerset is an unincorporated community and census-designated place (CDP) located within Franklin Township, in Somerset County, New Jersey, United States. As of the 2010 United States Census, the CDP's population was 22,083. Somerset housed one of the first Marconi Wireless Stations in the United States. According to the United States Census Bureau, the CDP had a total area of 6.444 square miles (16.692 km2), including 6.327 square miles (16.388 km2) of land and 0.117 square miles (0.304 km2) of water (1.82%)....
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$67,661 to $91,216
Somerset, New Jersey area prices
were up 1.5% from a year ago

Clinical Research Coordinator in Monterey, CA
Coordinators often become the front line for patients because they feel more comfortable with us.
November 07, 2019
Clinical Research Coordinator in Bakersfield, CA
If you have a medical experience you may need a certificate program to work as a CRC bt if there is none then you will need an education program that covers all the required medical and research coursework in clinical research.
October 27, 2019
Clinical Research Coordinator in New Bedford, MA
If you’re looking for a job you can complete at home that lets you use your organizational and leadership skills, a career in clinical research coordination could be for you.
October 09, 2019