CLINICAL RESEARCH COORDINATOR

2 weeks ago


Wildwood MO USA, United States Headlands Research Full time
Overview

Clinical Research Professionals (CRP) is a dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through the advancement of new drug therapies and medical devices. We have recently partnered with the Headlands Research Network to provide best in class clinical trial services.

This is a full time position based at our office in St. Louis, MO

The Role

Clinical Research Professionals is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.

Responsibilities

* Comprehend study design of each protocol that is assigned
* Obtain informed consent from study participants
* Perform procedures in compliance with the study protocol
* Screen study subjects according to specific protocol requirements
* Collect and record study data in source documents via electronic system (CRIO)
* Manage study related activities
* Ensure adherence to protocol requirements
* Review laboratory data
* Assess and document compliance
* Manage investigational product
* Assess, record, and report Adverse Events as outlined in the protocol
* Manage/train ancillary staff

Qualifications

* Experience and training in conducting clinical trials with knowledge of ICH GCP
* Licensed Nurse in Missouri is a plus
* IV Certification is a plus
* Degree in a health or scientific related program strongly preferred
* Excellent interpersonal and communication skills: Able to interact effectively with professional and administrative staff, sponsor and regulatory representatives.
* Compassion for patients (study participants)
* Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing lab specimens
* Excellent written & oral communication skills
* Have a passion for clinical research and helping people
* Experience with CRIO (Clinical Trial Management System) is a plus
* Experience with administering vaccines is a plus

  • Wildwood, MO 63005, USA, United States Headlands Research Full time

    OverviewClinical Research Professionals (CRP) is a dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through the advancement of new drug therapies and medical devices. We have recently partnered with...


  • Wildwood, MO 63005, USA, United States Headlands Research Full time

    OverviewClinical Research Professionals (CRP), a Headlands Research site, is a privately owned dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through advancement of new drug therapies and medical...


  • Wildwood, MO 63005, USA, United States Headlands Research Full time

    Clinical Research Professionals (CRP), a Headlands Research site,  is a privately owned dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through advancement of new drug therapies and medical...


  • Chesterfield, MO, United States Headlands Research Full time

    Overview Clinical Research Professionals (CRP) is a dedicated research center that provides a network of physicians who work collaboratively in conducting clinical research trials. Our team consists of experienced research professionals helping to improve lives through the advancement of new drug therapies and medical devices. We have recently partnered...


  • Wildwood, United States Medix Full time

    Summary:The research assistant is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of...


  • Kansas City, MO 64126, USA, United States Saint Luke's Health System Kansas City Full time

    Job DescriptionThe Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol and the primary activities include assisting in the evaluation of new protocols for feasibility at the site preparing the site for conduct of the study such as establishing study files and...


  • Kansas City, MO 64126, USA, United States Saint Luke's Health System Kansas City Full time

    Job DescriptionSupervise direct mentor and train clinical research nurses for Oncology research programs. Supervise oncology research clinical compliance following standardization and organization processes for all SLHS research programs. Maintain relationships with medical staff in assigned product line and use this knowledge to take the lead in research...


  • Kansas City, MO 64126, USA, United States University of Kansas Medical Center Full time

    Department:SOM KC Internal Medicine - Pulmonary, Critical Care, and Sleep Medicine* ----Pulmonary and Critical Care MedicinePosition Title:Clinical Research Assistant- PulmonaryJob Family Group:Professional StaffJob Description Summary:The Clinical Research Assistant assists in entry level clinical research activities including collecting information from...


  • Kansas City, MO 64126, USA, United States St. Luke's of Kansas City Full time

    Job DescriptionThe Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol. The primary activities include, but are not limited to:* Assisting in the evaluation of new protocols for feasibility at the site* Preparing the site for conduct of the study such as...


  • Chicago, IL, USA, United States Alliance for Clinical Trial in Oncology Foundation Full time

    The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation created to enhance and expand the ability of the Alliance for Clinical Trials in Oncology (Alliance) to conduct cancer clinical research and address important treatment questions through large-scale clinical trials. Through efforts of the Foundation in support of the...


  • Tampa, FL 33602, USA, United States The Tampa General Hospital Foundation Inc Full time

    Department ProfileThe 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...


  • 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...


  • 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...


  • Kansas City, MO, United States University of Kansas Medical Center Full time

    Department: SOM KC Internal Medicine - Pulmonary, Critical Care, and Sleep Medicine * ---- Pulmonary and Critical Care Medicine Position Title: Clinical Research Assistant- Pulmonary Job Family Group: Professional Staff Job Description Summary: The Clinical Research Assistant assists in entry level clinical research activities including collecting...


  • Aurora, CO 80041, USA, United States University of Colorado Full time

    University of Colorado Anschutz Medical CampusSchool of Medicine | Department of Medicine | Division of RheumatologyOfficial Title: Research Services Principal Clinical Science ProfessionalWorking Title: Clinical Research NursePosition: #00817289 - Requisition: #31662Job Summary:The Research Services Principal Professional (Clinical Research Nurse) is a 100%...


  • San Antonio, TX 78245, USA, United States UT Health San Antonio Full time

    Under limited supervision, responsible for actively facilitating clinical research by administering and monitoring treatment or research protocols. Coordinates and participates in clinical research studies conducted by principal investigator; coordinates and participates in a variety of complex activities involved in the recruitment, collection, compilation,...


  • Kansas City, MO, United States St. Luke's of Kansas City Full time

    Job Description The Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol. The primary activities include, but are not limited to: * Assisting in the evaluation of new protocols for feasibility at the site * Preparing the site for conduct of the study such...


  • Kansas City, MO, United States Saint Luke's Health System Kansas City Full time

    Job Description The Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol and the primary activities include assisting in the evaluation of new protocols for feasibility at the site preparing the site for conduct of the study such as establishing study files...


  • Kansas City, MO, United States Saint Luke's Health System Kansas City Full time

    Job Description Supervise direct mentor and train clinical research nurses for Oncology research programs. Supervise oncology research clinical compliance following standardization and organization processes for all SLHS research programs. Maintain relationships with medical staff in assigned product line and use this knowledge to take the lead in research...


  • New Haven, CT 06501, USA, United States Yale University Full time

    Essential Duties1. Evaluates and assesses subject's suitability for inclusion in studies; develops and modifies procedures according to study findings; recommends changes to the study protocol to coincide with study goals and objectives. 2. Develops and implements procedures and data quality assurance standards for safety monitoring components of studies. 3....