We have other current jobs related to this field that you can find below

  • Regulatory Affairs Coordinator

    4 weeks ago

    Staten Island, United States Evolution Research Group Full time

    Job DetailsJob Location LOC022 RBA Richmond Behavioral Associates - Staten Island, NY Salary Range $26.00 - $32.00 Hourly Regulatory CoordinatorJob Title: Regulatory Affairs CoordinatorLocation: Staten Island, NYAbout us: ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services...

  • Clinical Trial Support Specialist

    6 days ago

    Staten Island, New York, United States Evolution Research Group Full time

    Position: Clinical Trial Support Specialist, Inpatient Unit About Evolution Research Group: Evolution Research Group is a prominent U.S.-based, privately owned clinical research organization specializing in clinical development services, particularly in the realm of neuroscience drug development. With a network of 20 fully owned clinical facilities and 4...

  • Clinical Trial Support Specialist

    6 days ago

    Staten Island, New York, United States Evolution Research Group Full time

    Position: Clinical Trial Support Specialist, Inpatient Unit Overview: Evolution Research Group is a privately owned clinical research organization specializing in both early and late-stage neuroscience drug development. We operate a network of clinical sites dedicated to conducting comprehensive phase I-IV clinical research studies. With a robust...

  • Research Nurse

    1 month ago

    Staten Island, United States Northwell Health Full time

    Job Description Assists in research projects involving direct patient care with adherence to established protocols so that projects are carried out as directed by the Institutional Review Board (IRB). Works within scope of practice to perform clinical procedures. Collaborates with physicians and clinical/ancillary team members to ensure integrity of research...

  • Clinical Trials Manager

    6 days ago

    Staten Island, New York, United States Northwell Health Full time

    Clinical Trials ManagerAs a key player in our research initiatives, the Clinical Trials Manager is responsible for the comprehensive coordination and oversight of clinical research studies. This role involves actively managing the recruitment of participants and ensuring adherence to regulatory standards and protocols.Key Responsibilities:Coordinate and...

  • Principal Investigator Research

    4 months ago

    Staten Island, United States Happy Day Health Full time

    We are seeking Board Certified Physician to join our team as a Principal Investigator. As a key member of our research company, you will play a crucial role in overseeing and conducting clinical trials. In this role you will ensure protocols adhere to regulatory requirements and ethical standards, supervise data collection, collaborate with cross-functional...

  • Research Nurse

    1 month ago

    Staten Island, New York, United States Northwell Health Full time

    Job DescriptionAssists in research projects involving direct patient care with adherence to established protocols so that projects are carried out as directed by the Institutional Review Board (IRB). Works within scope of practice to perform clinical procedures. Collaborates with physicians and clinical/ancillary team members to ensure integrity of research...

  • Front Office Coordinator

    6 days ago

    Staten Island, New York, United States Evolution Research Group Full time

    Detalles del TrabajoUbicación del Trabajo RBA Richmond Behavioral Associates - Staten Island, NY Rango Salarial $25.00 Recepcionista/Coordinador de OficinaTítulo: Coordinador de OficinaUbicación: Staten IslandAcerca de nosotros: Evolution Research Group es una destacada empresa estadounidense, privada e independiente, especializada en sitios de...

  • Esthetics Clinic Education Coordinator

    6 days ago

    Staten Island, New York, United States Paul Mitchell Schools Full time

    Paul Mitchell Schools is on the lookout for a dedicated Esthetics Clinic Education Coordinator to enhance our vibrant community. With a network of over one hundred schools across the nation, we pride ourselves on our rapid growth and our commitment to a culture that emphasizes kindness and inclusivity. Our environment fosters exceptional learning...

  • Clinical Research Manager- 232996

    2 days ago

    new york city (staten island), United States Medix™ Full time

    We are seeking a skilled clinical research leadership professional to work as a Clinical Operations Manager at a clinical research site in Staten Island, NY! The Clinical Operations Manager (COM) is responsible for the oversight of all aspects of Clinical Trial Team activities at a clinical trial site. The COM, in concert with the Site Director and Principal...

  • Oncology Clinical Research Specialist

    6 days ago

    Hilton Head Island, South Carolina, United States St. Josephs Candler Full time

    Position OverviewThe Oncology Clinical Research Coordinator (CRC) is a dedicated research expert collaborating with the clinical Principal Investigator (PI) on various research initiatives. The CRC is tasked with managing and organizing the daily operations of clinical trials related to Cancer Care Delivery Research (CCDR) and cancer control studies as...

  • Medical Front Desk Receptionist

    2 months ago

    Staten Island, United States Evolution Research Group Full time

    Job DetailsJob Location LOC022 RBA Richmond Behavioral Associates - Staten Island, NY Salary Range $18.00 - $25.00 Receptionist/Front DeskTitle: Receptionist Location: Staten IslandAbout 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...

  • Cancer Care Research Coordinator

    6 days ago

    Hilton Head Island, South Carolina, United States St. Josephs Candler Full time

    Position OverviewThe Oncology Clinical Research Coordinator (CRC) plays a vital role in supporting the clinical Principal Investigator (PI) in the management of ongoing research initiatives. The CRC is tasked with the facilitation and organization of daily clinical trial operations related to Cancer Care Delivery Research (CCDR) and cancer control studies as...

  • Clinical Research Nurse

    2 months ago

    Wilmington Island, United States Memorial Health University Medical Center Full time

    Description IntroductionLast year our HCA Healthcare colleagues invested over 156,000 hours volunteering in our communities. As a(an) Clinical Research Nurse with Memorial Health University Medical Center you can be a part of an organization that is devoted to giving back!BenefitsMemorial Health University Medical Center, offers a total rewards package that...

  • Clinical Research Nurse

    1 week ago

    Wilmington Island, GA, United States Memorial Health University Medical Center Full time

    Description Introduction Last year our HCA Healthcare colleagues invested over 156,000 hours volunteering in our communities. As a(an) Clinical Research Nurse with Memorial Health University Medical Center you can be a part of an organization that is devoted to giving back! Benefits Memorial Health University Medical Center, offers a total rewards...

  • Clinical Trials Coordinator for Oncology

    1 day ago

    Hilton Head Island, South Carolina, United States St. Josephs Candler Full time

    Position OverviewThe Oncology Clinical Research Coordinator (CRC) plays a pivotal role in the execution of clinical trials under the guidance of the Principal Investigator (PI). This professional is tasked with the organization and management of daily activities related to Cancer Care Delivery Research (CCDR) and cancer control trials as directed by the...

  • Clinical Supervisor for Justice Initiatives

    6 days ago

    Staten Island, New York, United States Community Health Action of Staten Full time

    Position OverviewTitle: Clinical Coordinator, Alternatives to IncarcerationDepartment: Health Care CoordinationReports To: Director of Justice InitiativesPosition Status: Full-TimeFLSA Status: Non-exemptCompensation and Benefits: The salary range for this position typically falls between $55,000 and $60,000 annually, based on relevant experience and...

  • Clinical Audiologist

    6 days ago

    Staten Island, New York, United States Northwell Health Full time

    Position OverviewThe Audiologist is responsible for conducting comprehensive audiological assessments across various age demographics, including specialized evaluations. This role involves ensuring the proper fitting of hearing devices and determining the suitability of rehabilitative services. The Audiologist also provides essential counseling to patients...

  • Clinical Research Nurse

    4 weeks ago

    Wilmington Island, GA, United States Memorial Health University Medical Center Full time

    Job DescriptionDescription IntroductionLast year our HCA Healthcare colleagues invested over 156,000 hours volunteering in our communities. As a(an) Clinical Research Nurse with Memorial Health University Medical Center you can be a part of an organization that is devoted to giving back!BenefitsMemorial Health University Medical Center, offers a total...

  • Clinical Nutrition Specialist

    5 days ago

    Staten Island, New York, United States New York State Civil Service Full time

    Position Overview:This role involves overseeing clinical nutrition services under the guidance of the Nutrition Services Administrator 2. The successful candidate will be responsible for ensuring that nutritional records accurately reflect the dietary needs of individuals and comply with relevant regulations.Key Responsibilities:Manage and coordinate medical...

Clinical Research Coordinator-(Psych)

2 months ago

Staten Island, United States Evolution Research Group Full time
Job Details

Job Location
LOC022 RBA Richmond Behavioral Associates - Staten Island, NY

Salary Range
$24.00 - $35.00

CRC-FT

Title: Clinical Research Coordinator, Psych exp. preferred

Location: Staten Island, NY

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)