Current jobs related to Clinical Research Coordinator- 232165 - orlando - Medix™


  • Orlando, Florida, United States CHARTER RESEARCH Full time

    Job Title: Clinical Research CoordinatorJob Summary:Charter Research is seeking a highly skilled Clinical Research Coordinator to support the day-to-day operations of clinical trials. As a key member of our team, you will be responsible for ensuring the successful performance of clinical research studies.Responsibilities:* Assist in the performance of...


  • Orlando, Florida, United States Charter Research Full time

    Job Title: Prescreen CoordinatorCharter Research is a leading clinical research company based in The Villages and Orlando, FL, seeking a skilled Prescreen Coordinator to join our team.Job Summary:The Prescreen Coordinator will work closely with our clinical research team to assess potential new patients for optimal trial placement upon their first visit to...


  • Orlando, Florida, United States CHARTER RESEARCH Full time

    Job Title: Prescreen CoordinatorCharter Research is a leading clinical research company seeking a skilled Prescreen Coordinator to join our team. As a Prescreen Coordinator, you will play a critical role in assessing potential new patients for optimal trial placement and providing exceptional patient experience.Key Responsibilities:Conduct thorough...


  • Orlando, Florida, United States CHARTER RESEARCH Full time

    Job OverviewCharter Research is a leading clinical research company seeking a highly skilled Prescreen Coordinator to join our team in Orlando, FL.As a Prescreen Coordinator, you will play a critical role in assessing potential new patients for optimal trial placement and providing exceptional patient experience.This is an exciting opportunity to work in a...


  • Orlando, Florida, United States Charter Research Full time

    Company OverviewCharter Research is a leading clinical research company dedicated to discovering future medicines. We are seeking a skilled Prescreen Coordinator to join our team in Orlando, FL.Job SummaryThe Prescreen Coordinator will work closely with our clinical research team to assess potential new patients for optimal trial placement. This role...


  • Orlando, Florida, United States CHARTER RESEARCH Full time

    Job Title: Clinical Research DirectorCharter Research is seeking an experienced and motivated Clinical Research Director to lead our Patient Engagement Team at our clinical research site in Orlando, Florida.Job Summary:We are looking for a seasoned professional to oversee the development and implementation of patient engagement initiatives, staff standards,...


  • Orlando, Florida, United States Actalent Full time

    Job Title:Clinical Research CoordinatorThe Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects.The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI), Sub-Investigators (Sub-I),...


  • Orlando, Florida, United States Medix Full time

    Medix is seeking a highly skilled Clinical Research Coordinator to join their team.Key Responsibilities:Coordinate clinical trials and studiesManage data entry and validationEnsure compliance with regulatory requirementsCollaborate with research teamsRequirements:2+ years of experience as a Clinical Research CoordinatorWork Schedule:Monday through Friday,...


  • Orlando, Florida, United States Actalent Full time

    Job SummaryWe are seeking a highly skilled Neurology Clinical Research Coordinator II to join our team at Actalent. As a key member of our research team, you will be responsible for coordinating clinical trials and research studies in the field of neurology.Key ResponsibilitiesConduct patient recruitment, screening, and eligibility assessment for research...


  • Orlando, United States Actalent Full time

    Work Site This is a fully on-site position in Orlando, Florida Qualifications MUST have Neurology experience within the Clinical Research space Bachelor’s degree in Healthcare Administration, Research, or related field with a minimum of 3 years’ of Clinical Research experience Neurology Clinical Research Coordinator II Conducting...


  • Orlando, United States Actalent Full time

    Work Site This is a fully on-site position in Orlando, Florida Qualifications MUST have Neurology experience within the Clinical Research space Bachelor’s degree in Healthcare Administration, Research, or related field with a minimum of 3 years’ of Clinical Research experience Neurology Clinical Research Coordinator II Conducting...


  • Orlando, United States DirectEmployers Full time

    Job Title: Clinical Research CoordinatorJob Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...


  • Orlando, United States DirectEmployers Full time

    Job Title: Clinical Research CoordinatorJob Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...


  • Orlando, United States AdventHealth Full time

    Clinical Research Coordinator II -RN – AdventHealth Orlando All the benefits and perks you need for you and your family: -Benefits from Day One-Paid Days Off from Day One-Student Loan Repayment Program-Career Development -Whole Person Wellbeing Resources-Mental Health Resources and Support-Pet Insurance* -Debt-free Education* (Certifications and Degrees...


  • Orlando, Florida, United States AdventHealth Full time

    Job SummaryAdventHealth is seeking a Clinical Research Supervisor to oversee the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. The ideal candidate will have a strong background in clinical research, excellent leadership skills, and the ability to work...


  • Orlando, Florida, United States AdventHealth Full time

    Job Title: Clinical Research SupervisorAdventHealth is seeking a highly skilled Clinical Research Supervisor to join our team. As a Clinical Research Supervisor, you will be responsible for overseeing the conduct of clinical trials, ensuring compliance with regulatory requirements, and providing guidance to research staff.Key Responsibilities:Supervise and...


  • Orlando, Florida, United States Medix™ Full time

    Clinical Research CoordinatorMedix is seeking a highly skilled Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating and overseeing all aspects of clinical trials, ensuring compliance with ethical standards, institutional policies, and regulatory requirements.Key...


  • Orlando, Florida, United States AdventHealth Full time

    Job SummaryWe are seeking a highly skilled Clinical Research Supervisor to join our team at AdventHealth Orlando. As a Clinical Research Supervisor, you will be responsible for overseeing the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines.Key...


  • Orlando, United States Nemours Full time

    Clinical Research Nurse in Oncology supporting NCCBD (Nemours Center for Cancer & Blood Disorders) - coordinates, implements and completes clinical research studies and/or clinical trials by assisting in screening oncology patients, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures,...

  • Prescreen Coordinator

    2 months ago


    orlando, United States Charter Research Full time

    COMPANY DESCRIPTIONCharter Research is a highly experienced and quickly growing clinical research company, based in The Villages and Orlando, FL that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is locally owned and prides itself on providing exceptional patient experience to our participants, as...

Clinical Research Coordinator- 232165

2 months ago


orlando, United States Medix™ Full time

Position Overview:

In this role you will ensure IRB approved protocols are implemented and followed; execute the

informed consent process and monitor patient status and safety; collect and organize research

data; schedule and conduct study-specific training and site in-services to study related staff on

new or amended protocols, and educate patients and their families about treatments and

possible side effects. The Clinical Research Coordinator must also be able to perform clinical

tasks.


Responsibilities:

● Site preparation.

● Obtaining informed consent, patient screening and recruitment.

● Patient enrollment, and conducting study visits.

● Maintaining and dispensing study product and supplies.

● Completing and ensuring the quality of case report forms.

● Maintaining source documents

● Ensuring site quality.

● Maintain a thorough and meticulous working knowledge of protocol schemas and requirements.

● Collaborate with physicians to maintain strict protocol adherence and serve as a resource for members of staff.

● Writes patient information sheet for clinical studies for submission to IRB, as well as complete the necessary documents for IRB admission in a timely fashion.

● Participate in the development and implementation of patient educational materials.

● Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well a complete the necessary documents for IRB submission in a timely fashion.

● Review research and administrative documents to determine action items, prioritizing and tracking action items.

● Responsible for completion, submission and tracking of regulatory documents to the IRB.

● Maintain and update research fund accounting files, research billing, budgets and transfer of funds.

● Respond to correspondence, data and informational requests.

● Analysis of statistical, resource, performance and budget data and generation of reports.


Qualifications:

● 1-2 years of Clinical Research Coordinator (CRC) experience or relevant experience