Clinical Research Associate jobs in Vermont

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Central Clinical Data Coordinator
  • DM Clinical Research
  • Cambridge, VT CONTRACTOR
  • Central Clinical Data Coordinator

    A Central Clinical Data Coordinator works to coordinate and implement data collection for various studies, focusing on the day-to-day operations, including, monitoring the completion of project-related tasks, maintaining study-related procedures to ensure protocol and regulatory compliance. In a centralized role, the CCDC may be working on multiple trials at once, completing data capture, eDiary, and other data-related tasks.


    DUTIES & RESPONSIBILITIES
    • Collect, enter, analyze, and manage data from clinical studies
    • Maintain training and understanding of FDA, GCP, GDP, IATA, and Sponsor specified systems/processes
    • Maintain working knowledge of current FDA GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
    • Ensure the quality of data submitted from assigned study sight, while, assuring timely entry into corresponding study database, submission of data and appropriate reporting and follow-up of data collection
    • Ensure the internal processes follow the study protocol, amendment(s), while being in line with
    • GCP, GDP and regulatory guidelines
    • Ensure data collected is accurate, legible, contemporaneous, original, authentic, and complete
    • Resolve any discrepancies, queries and events in-line with company and study protocols
    • Complete eDiary functions
    • Document clinical trial progress to ensure completeness of documentation and adherence to trial and/or project timelines
    • Contribute to, and/or generate requested reports for management
    • Be accountable for data collection process
    • Participate in required trainings as set forth by the company, department, sponsors, and trials
    • Being prepared for and available at all the necessary company meetings and monitoring visits for their assigned protocols
    • Submitting required administrative paperwork per company timelines
    • Any other matters as assigned by management related to data collection for responsible trials

    KNOWLEDGE & EXPERIENCE

    Education:
    • High school diploma required
    • Associate degree or Bachelor’s preferred
    • Experience:
    • Experience with medical terminology is a plus
    • Experience with data entry is a plus
    Credentials:
    • N/A
    Knowledge and Skills:
    • Strong knowledge of Google Suite products, Clinical Databases and other computer-related software
    • Excellent oral and written communication skills
    • Excellent planning and organizational skills with effective time management
    • Excellent interpersonal skills
    • Meticulous, independent, and capable of working with minimal supervision
    • Excellent data handling and analyzing skills
    • Initiative and problem-solving skills
    • Thorough understanding of clinical research principles and processes. Ability to input into process initiatives, and procedures related to Good Clinical Practices (GCP).
  • 1 Day Ago

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Patient Engagement Project Specialist
  • DM Clinical Research
  • Cambridge, VT CONTRACTOR
  • Patient Engagement Project SpecialistThe Patient Engagement Project Specialist will be dedicated to drive patient enrollment, patient engagement and patient experience initiatives for clinical researc...
  • 7 Days Ago

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Digital Marketing Specialist
  • DM Clinical Research
  • Cambridge, VT CONTRACTOR
  • Digital Marketing SpecialistThis position requires a go-getter attitude, attention to detail, and creative thinking. Facebook and Google Ads experience is required for this role. The ideal candidate w...
  • 1 Month Ago

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Financial Planning & Analyst
  • DM Clinical Research
  • Cambridge, VT FULL_TIME
  • Financial Analyst A Financial Planning Analyst is a central liaison between the corporate and operations teams. They are also in charge of management planning and decision-making by identifying, maint...
  • 1 Month Ago

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Study Start Up Specialist
  • DM Clinical Research
  • Cambridge, VT CONTRACTOR
  • Study Start-Up Specialist Study Start-Up Specialist will be an integral part of the project management team and help manage the portfolio of active and future studies Business Development has in the p...
  • 1 Month Ago

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Business Services Coordinator
  • DM Clinical Research
  • Cambridge, VT CONTRACTOR
  • Business Services CoordinatorThe Business Services Coordinator will play a crucial role in ensuring the seamless flow of materials and supplies across the supply chain by establishing and maintaining ...
  • 1 Month Ago

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Clinical Research Associate/Sr. Clinical Research Associate
  • Curevo Inc.
  • Bothell, WA
  • The Clinical Research Associate/Sr. Clinical Research Associate assists the clinical operations team in the oversight, o...
  • 4/19/2024 12:00:00 AM

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Clinical Research Associate
  • Thermo Fisher Scientific
  • Wilmington, NC
  • Job Description Company Name: PPD Development, L.P. Position Title: Clinical Research Associate Location: 929 North Fron...
  • 4/19/2024 12:00:00 AM

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Clinical Research Associate
  • Thermo Fisher Scientific Inc.
  • Wilmington, NC
  • Job Description Company Name: PPD Development, L.P. Position Title: Clinical Research Associate Location: 929 North Fron...
  • 4/19/2024 12:00:00 AM

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Clinical Research Associate I
  • Abbott Laboratories
  • Alameda, CA
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 4/18/2024 12:00:00 AM

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Clinical Research Associate
  • Mcinnis Inc.
  • Ridgefield, CT
  • The Clinical Research Associate will support clinical research activities within research sites that are actively partic...
  • 4/18/2024 12:00:00 AM

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Clinical Research Associate
  • McInnis, Inc.
  • Ridgefield, CT
  • The Clinical Research Associate will support clinical research activities within research sites that are actively partic...
  • 4/17/2024 12:00:00 AM

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Clinical Research Associate
  • Abbott Laboratories
  • South Portland, ME
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 4/16/2024 12:00:00 AM

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Clinical Research Associate I
  • Abbott Laboratories
  • Alameda, CA
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 3/15/2024 12:00:00 AM

Vermont is located in the New England region of the Northeastern United States and comprises 9,614 square miles (24,900 km2), making it the 45th-largest state. It is the only state that does not have any buildings taller than 124 feet (38 m). Land comprises 9,250 square miles (24,000 km2) and water comprises 365 square miles (950 km2), making it the 43rd-largest in land area and the 47th in water area. In total area, it is larger than El Salvador and smaller than Haiti. It is the only landlocked state in New England, and it is also the easternmost and the smallest in area of all landlocked sta...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$67,019 to $88,520

Clinical Research Associate in Vista, CA
Represents Global Clinical Affairs on multifunctional teams tasked with preparing responses to regulatory agencies.
May 02, 2023
Clinical Research Associate in Stockton, CA
Document informed consent discussion and obtain signatures per protocol, federal, state and institutional requirements.
April 20, 2023
Clinical Research Associate in Stamford, CT
Responds flexibly to changing business demands and opportunities, proactively looking for ways to contribute.
May 09, 2023
Participate in monitoring visit report review process in order to maintain oversight of clinical monitoring quality and adherence to protocol and established processes and plans.
December 03, 2022