Jobs
>
Columbus

    Clinical Research Coordinator II - Columbus, United States - Nationwide Children's Hospital

    Nationwide Children's Hospital
    Nationwide Children's Hospital Columbus, United States

    1 week ago

    Default job background
    Description
    Overview


    The Nahata Lab is looking for a Clinical Research Coordinator II to support our mission of providing efficient coordination of diverse behaviorally-focused clinical research, including behavioral intervention trials and observational research.

    The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures.

    These elements include but are not limited to; start-up activities, launch activities, day to day management of a study, data coding, analysis, report generation, and study closure activities.

    The CRC II also trains and mentors other clinical research staff to ensure consistency in study management and coordination activities.

    Why Nationwide Children's Hospital?

    The moment you walk through our doors, you feel it. When you meet our patient families, you believe it. And when you talk with anyone who works here, you want to be part of it. Welcome to Nationwide Children's Hospital, Where Passion Meets Purpose.

    Here, Diversity, Equity and Inclusion are integrated into our core values and practices. We are passionate about building, sustaining and evolving an inclusive and equitable environment.

    We are seeking individuals who live these values and want to share their experiences and efforts in support of our collective mission.

    We're 14,000 strong.

    And it takes every one of us to improve the lives of the kids we care for, and the kids around the world we'll never meet.

    Kids who live healthier, fuller lives because of the knowledge we share.

    We know it takes a Collaborative Culture to deliver on our promise to provide the very best, innovative care and to foster new discoveries, made possible by the most groundbreaking research.

    Anywhere.

    Ask anyone with a Nationwide Children's badge what they do for a living. They'll tell you it's More Than a Job. It's a calling. It's a chance to use and grow your talent to make an impact that truly matters. Because here, we exist simply to help children everywhere.

    Nationwide Children's Hospital. A Place to Be Proud.

    Responsibilities


    Essential Job Functions:

    • Conducts clinical studies as outlined in the study protocol; discerns critical elements of the protocol to ensure participant safety throughout study; adheres to good clinical practices.
    • Interact with research participants, Principal Investigators, and hospital departments in-person, virtually, and over the phone.
    • Recruits, consents and enrolls participants according to ICH/GCP regulations, and participant's rights through institutional IRB, federal and state regulations; ensures the participant meets inclusion/exclusion criteria; answers questions related to the protocol procedures as applicable; acts as a patient/family advocate.
    • Coordinates and schedules participant study visits with study partners (e.g., other hospital services, the PI/sub-I, community partners, parallel studies).
    • Collects and manages protocol required data such as standardized and semi-structured assessments, observational or technology assisted data (e.g., Actigraphy), biological specimens, and archival data; scores data according to established procedures.
    • Performs study procedures according to recognized skill level and certifications and within the local and federal regulations and guidelines; collects, processes and ships human specimens and/or data for use in research studies per the IRB approved protocol.
    • Identifies study implementation and/or study management issues and works with the study team to develop and implement solutions to ensure study progress and success.
    • Assists with the study recruitment plan and manages participant incentive disbursement via established procedures; manages all screening, enrollment and study participation logs; provides recruitment summaries throughout the study.
    • Creates source documents and/or databases that facilitate systematic data collection and/or aid in protocol execution, management. and record keeping; and conducts accurate and timely participant data collection.
    • Assists with study database development to maintain study data in de-identified format, according to recognized skill level; accurately completes data collection forms.
    • Trains, mentors, and educates other study personnel with regards to study-specific responsibilities and keeps written documentation of this training.
    • Alerts the investigator or manager when the participant's safety is in jeopardy, there is a protocol deviation, or when the participant requests premature study termination.
    • Responsible for maintenance of IRB records and essential documents.
    • Completes data coding/scoring and statistical analyses as directed by the Principal Investigator. Creates visual representations of analyzed data and collaborates on dissemination of research results.

    Note:
    Regular, reliable and

    consistent attendance is an essential job function. Employees are expected to perform work as scheduled. Please see the physical requirements for this position listed below.

    Qualifications

    Knowledge, Skills & Abilities:

    Education Requirement:

    • Bachelor's or Master's degree in psychology, public health, or other health or clinical research related fields.
    • Certifications: CRA/CRC certification preferred.

    Skills:

    • Experience and interest in working with diverse populations.
    • Understanding of medical terminology and clinical trials preferred.
    • Working knowledge of PCs and word processing and data management software.
    • Demonstrated analytical skills with accuracy and attention to detail.
    • Goal-oriented and self-directive, ability to manage multiple complex projects independently.
    • Demonstrated independence and responsibility, including effective problem solving, and demonstrated ability to effectively balance multiple priorities.
    • Excellent verbal and written communication skills.
    • Strong organizational and interpersonal, including the ability to engage participants effectively over the telephone and in person.
    • Ability to actively participate as a team player and to work collaboratively with research participants, supervisors, and coworkers.
    • Flexible hours are required to accommodate data collection during some evening and weekend hours.

    Experience:
    Minimum of 2 years of experience in clinical research or health care field.


    The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification.

    It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.

    EOE M/F/Disability/Vet
  • EVOLUTION RESEARCH GROUP

    Clinical Research Coordinator

    1 week ago

    EVOLUTION RESEARCH GROUP Columbus, United States

    Job Details · Job Location · LOC019 OCT Ohio Clinical Trials - Columbus, OH · CRC · Title: Clinical Research Coordinator · Location: Columbus, OH · About us: · ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical devel ...

  • Ohio State University Wexner Medical Center

    Clinical Research Coordinator

    3 weeks ago

    Ohio State University Wexner Medical Center Columbus, United States

    Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Division of Endocrinology, Diabetes and Metabolism; assists with assessi ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The Clinical Research Coordinator I's primary responsibility is managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but ...

  • Evolution Research Group

    Clinical Research Coordinator

    1 day ago

    Evolution Research Group Columbus, United States

    Job Details · Job Location · LOC019 OCT Ohio Clinical Trials - Columbus, OH · CRC · Title: Clinical Research Coordinator · Location: Columbus, OH · About us: · ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical de ...

  • Medavie Health Services

    Clinical Research Coordinator

    1 day ago

    Medavie Health Services Columbus, United States

    About the Role · The Clinical Research Coordinator (CRC) is responsible for conducting and documenting clinical research and trials for the Research Division while adhering to Good Clinical Practice/ICH Guidelines and the Code of Federal Regulations. · What You'll Be Doing Admi ...

  • Ohio State University Wexner Medical Center

    Clinical Research Coordinator

    6 days ago

    Ohio State University Wexner Medical Center Columbus, United States

    Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Division of Pulmonary/Critical Care/Sleep Medicine in the Department of ...

  • Evolution Research Group

    Clinical Research Coordinator

    20 hours ago

    Evolution Research Group Columbus, United States

    Job DetailsJob LocationLOC019 OCT Ohio Clinical Trials - Columbus, OHCRCTitle: Clinical Research Coordinator Location: Columbus, OHAbout us:ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with ...

  • Medavie Health Services

    Clinical Research Coordinator

    2 days ago

    Medavie Health Services Columbus, United States

    About the Role The Clinical Research Coordinator (CRC) is responsible for conducting and documenting clinical research and trials for the Research Division while adhering to Good Clinical Practice/ICH Guidelines and the Code of Federal Regulations. What You'll Be Doing Administra ...

  • Columbus Community Clinical Oncology Program

    Clinical Research Coordinator

    1 week ago

    Columbus Community Clinical Oncology Program Columbus, United States

    Job Description · Job DescriptionDepartment: · Clinical Operations · Reports To: · Executive Director · Date Prepared: · April 29, 2024 · Position Summary: · Responsible for all aspects of clinical compliance and data quality for cancer treatment protocols within assigned resear ...

  • Columbus Community Clinical Oncology Program

    Clinical Research Coordinator

    1 week ago

    Columbus Community Clinical Oncology Program Columbus, United States

    Job Description · Job DescriptionDepartment: · Cancer Control / Cancer Care Delivery Research · Reports To: · Executive Director · Date Prepared: · April, 29, 2024 · Position Summary: · Responsible for all aspects of clinical compliance and data quality for assigned research base ...

  • Columbus Community Clinical Oncology Program

    Clinical Research Coordinator

    1 week ago

    Columbus Community Clinical Oncology Program Columbus, United States

    Job Description · Job DescriptionResponsible for all aspects of clinical compliance and data quality for cancer treatment protocols within assigned research bases. Maintains a thorough knowledge of assigned protocols and adheres to research principles and guidelines for meeting t ...

  • Trinity Health Corporation

    Oncology Clinical Research Coordinator

    1 week ago

    Trinity Health Corporation Columbus, United States

    Employment Type: · Full time · Shift: · Description: · In accordance with the Mission and Guiding Behaviors; the Research Coordinator is responsible for implementing and managing oncology clinical research projects across Mount Carmel Health System (MCHS). · * Serves as a resourc ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator II

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The Behavioral Trials Office is looking for a Clinical Research Coordinator II to support our mission of providing efficient coordination of diverse behaviorally-focused clinical research, including behavioral intervention trials and observational research. Our work sp ...

  • Trinity Health

    Oncology Clinical Research Coordinator

    1 week ago

    Trinity Health Columbus, United States

    **Employment Type:** · Full time · **Shift:** · **Description:** · In accordance with the Mission and Guiding Behaviors; the Research Coordinator is responsible for implementing and managing oncology clinical research projects across Mount Carmel Health System (MCHS). · - Serves ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator I

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The successful candidate will work with the Crerand Lab within the Center for Biobehavioral Health. Dr. Canice Crerand's research focuses on psychosocial and health outcomes in children, adolescents, and adults with congenital conditions including craniofacial conditio ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator II

    1 week ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The Clinical Research Coordinator II's primary responsibility is managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator II

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The Clinical Research Coordinator II's primary responsibility is managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements ...

  • The Ohio State University

    Clinical Research Coordinator-NE

    1 week ago

    The Ohio State University Columbus, United States

    Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr- If you have questions while submitting an application, please review these frequently asked questions. · Current Employees and Students: · If you are currently employed o ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator I

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · A full-time Research Coordinator is being recruited for a collaborative research team that is focused on examining family adjustment to children's life-threatening conditions, such as cancer. The successful candidate will contribute to ongoing work with children and ad ...

  • Nationwide Children's Hospital

    Clinical Research Coordinator I

    2 weeks ago

    Nationwide Children's Hospital Columbus, United States

    Overview · The Behavioral Trials Office is looking for a Clinical Research Coordinator I to support our mission of providing efficient coordination of diverse behaviorally-focused clinical research, including behavioral intervention trials and observational research. Our work spa ...