CLINICAL RESEARCH COORDINATOR

2 weeks ago

OH United States EVOLUTION RESEARCH GROUP Full time
Job Details

Job Location
LOC017 MCRC Midwest Clinical Research Center - Dayton, OH

Clinical Research Coordinator (CRC)

Title: Clinical Research Coordinator (CRC)

Location: Dayton, OH

Great benefits, competitive pay, matching 401k, apply today.

About us:

ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.

Job Description:

The Clinical Research Coordinator is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

General
  • Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
  • Assist to develop draft source documents and review the documents for accuracy and clarity prior to study start up.
  • Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
  • Manage studies with direct oversight from Site Director, and Principal Investigator to ensure compliance with protocol requirements.
  • Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
  • Contribute to the SOP review and development as delegated by the Site Director.

Study Management
  • Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
  • Attend the investigator meeting for each assigned protocol, as appropriate with directive from Site Director.
  • In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
  • Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
  • Review and obtain informed consent from with potential study volunteer
  • Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations
  • Maintain organized, accurate and complete study records
  • Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
  • Enter data as appropriate for protocol (paper-electronic data capture)
  • In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
  • Perform study close-out procedures.
  • Store study records appropriately.
  • Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives.

Skills and Qualifications:
  • Education and experience
    • High School Diploma or its equivalent; College degree preferred.
    • Two (2) to four (4) years of experience OR certification as a Clinical Research Coordinator
    • Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
    • Knowledgeable in medical terminology to communicate with physician office and laboratory staff.
    • Demonstrate the initiative to act independently, initiate activity as required and make appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
    • Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
  • Requirements
    • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
    • Excellent communication skills (interpersonal, written, verbal)
    • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

#HP

  • CLINICAL RESEARCH PROGRAM COORDINATOR NON-RN

    4 weeks ago

    , OH, United States PSG Global Solutions Full time

    Clinical Research Program Coordinator Non-RN - Requisition ID 2021-31287 Category. Research. Overview. Clinical Research Program Coordinator Non-RN - The Clinical Research Program Coordinator's primary responsibility is the overall administrative coo Clinical, Program, Research, Coordinator, Healthcare, Staffing, Children, Management

  • CLINICAL RESEARCH PROGRAM COORDINATOR NON-RN

    2 weeks ago

    Columbus, OH, United States PSG Global Solutions Full time

    Clinical Research Program Coordinator Non-RN - Requisition ID 2021-31260 Category. Research. Overview. Clinical Research Program Coordinator Non-RN - The Clinical Research Program Coordinator's primary responsibility is the overall administrative coo Clinical, Program, Research, Coordinator, Healthcare, Staffing, Children, Management

  • Clinical Research Nurse

    4 hours ago

    Monroe, NC, United States MONROE BIOMEDICAL RESEARCH LLC Full time

    IntroductionMonroe Biomedical Research is one of the highest-performing clinical research centers in the country, investigating therapies for the treatment of Asthma, COPD, Heart failure, Hypertension, Diabetes, COVID-19, Obesity, Major Depressive Disorder, and Opioid Use Disorder.. The company is preparing for an expansion of its operations within the next...

  • CLINICAL RESEARCH NURSE

    2 weeks ago

    , PA, United States Temple University Health System Full time

    Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety...

  • UNBLINDED CLINICAL RESEARCH NURSE

    2 weeks ago

    , OR, United States Headlands Research Full time

    OverviewAt Headlands Research, we are building a best in class clinical trial network. We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 15 clinical trial sites in the US and Canada...

  • CLINICAL RESEARCH NURSE

    3 days ago

    , MA, United States Massachusetts General Hospital Full time

    GENERAL SUMMARY/OVERVIEW STATEMENT:Under general direction of the Principal Investigator, the Research Study Nurse is responsible for specific aspects of designated research protocols and policies of the clinical studies.The Tearney Laboratory (www.tearneylab.org) at the Massachusetts General Hospital is a multidisciplinary research laboratory that invents,...

  • Clinical Research Nurse

    7 minutes ago

    , NY, United States Columbia University Full time

    * Job Type: Officer of Administration * Bargaining Unit: * Regular/Temporary: Regular * End Date if Temporary: * Hours Per Week: 35 * Standard Work Schedule: * Building: * Salary Range: $80,000 - $110,000 The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets,...

  • Clinical Research Nurse

    4 hours ago

    Philadelphia, PA, United States Temple University Health System Full time

    Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety...

  • Unblinded Clinical Research Nurse

    4 hours ago

    Portland, OR, United States Headlands Research Full time

    Overview At Headlands Research, we are building a best in class clinical trial network. We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 15 clinical trial sites in the US and...

  • Clinical Research Nurse

    3 hours ago

    Boston, MA, United States Partners Healthcare System Full time

    GENERAL SUMMARY/OVERVIEW STATEMENT: Under general direction of the Principal Investigator, the Research Study Nurse is responsible for specific aspects of designated research protocols and policies of the clinical studies. The Tearney Laboratory (www.tearneylab.org) at the Massachusetts General Hospital is a multidisciplinary research laboratory that...

  • Clinical Research Nurse

    5 hours ago

    Tampa, FL, United States The Tampa General Hospital Foundation Inc Full time

    Department Profile The TGH Cancer Institute Clinical Research Office is the centralized clinical research enterprise to support all Oncology research. As the hub for all cancer research activities, this office supports all aspects of research including but not limited to trial feasibility, activation, recruitment, and enrollment into Phase I-IV clinical...

  • Clinical Licensed Pool

    7 days ago

    Los Angeles, CA, United States Cambay Healthcare LLC Full time

    Location: 11800 Wilshire Boulevard Los Angeles, CA 90025Description:Float Location: 1919 Santa Monica Blvd.Required:BCLS certified from AHA or ARC3 years of clinical research experiencePreferred:6-12 months Oncology experienceSoCRA or ACRP certificationPhlebotomy certificationMA diploma from DAPIP accredited program or LVN licensed in CA\*\*Serve as lead...

  • Research Assistant

    3 days ago

    Houston, TX, United States Evolution Research Group Full time

    Title: Research AssistantLocation: Houston, TXAbout us:ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient...

  • Clinical Research Nurse II

    3 hours ago

    Philadelphia, PA, United States Temple University Health System Full time

    Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety...

  • CLINICAL RESEARCH NURSE

    3 weeks ago

    Cincinnati, OH 45201, USA, United States TriHealth, Inc. Full time

    Job Overview:Acts as the clinical research nurse for research studies in which TriHealth participates. Acts as a liaison between Study Sponsors, Study Monitors, Principal Investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a clinical research...

  • CLINICAL RESEARCH NURSE

    1 week ago

    Cincinnati, OH 45242, USA, United States TriHealth Full time

    Job DescriptionJob Overview:Acts as the clinical research nurse for research studies in which TriHealth participates. Acts as a liaison between Study Sponsors, Study Monitors, Principal Investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a...

  • Clinical Research Nurse II

    56 minutes ago

    Philadelphia, PA, United States Temple University Health System Full time

    Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety...

  • Clinical Research Nurse

    23 minutes ago

    Philadelphia, PA, United States Temple University Health System Full time

    Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety...

  • Clinical Research Nurse

    5 hours ago

    Chicago, IL, United States Northwestern University Full time

    Department: MED-Clinical Trials Unit Salary/Grade: EXS/8 Job Summary: Under general supervision and according to standard practice or general instruction, directly supports the research initiatives of the Bluhm Cardiovascular Institute Clinical Trials Unit. Collaborates with the physicians and clinical team in implementing investigator-initiated,...

  • PRN Infusion Nurse/EMT

    5 hours ago

    Lakeland, FL, United States Alcanza Clinical Research Full time

    PRN Infusion Nurse/EMT Department: Operations Employment Type: Contract Location: Accel Research Sites - Lakeland, FL Reporting To: colleen Figueroa Description Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong...