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Clinical Ethicist jobs in Florida

Clinical Ethicist offers guidance to patients, their families, and professional staff on ethical, legal and policy issues and concerns stemming from clinical interactions between health care professionals and patients. Provides guidance to the institutional ethics committee pertaining to policy formulation and educational and case review activities. Being a Clinical Ethicist develops institutional policies concerning ethical issues such as "do-not-resuscitate" and "withdrawal of life-support". Requires a master's degree or doctorate related to health ethics. Additionally, Clinical Ethicist typically reports to a manager or head of a unit/department. To be a Clinical Ethicist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (Copyright 2024 Salary.com)

Recently Added Clinical Ethicist jobs

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Clinical Research Coordinator
  • Alcanza Clinical Research
  • Lakeland, FL FULL_TIME
  • Department: Operations

    Employment Type: Full Time

    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 presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

    We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.

    Essential Job Duties

    In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:

  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:
    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
    • Filing SAE/Deviation reports to Sponsor and IRB as needed;
    • Documenting and reporting adverse events;
    • In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:

    Under The Direction Of The Site Manager/Director And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With FDA, GCP, ICH Regulations And Guidelines

    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
    • Filing SAE/Deviation reports to Sponsor and IRB as needed;
    • Documenting and reporting adverse events;
    • Reporting non-compliance to appropriate staff in timely manner;
    • Maintaining positive and effective communication with clients and team

    members;

    • Always practicing ALCOAC principles with all documentation;
    • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
    • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
    • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
    • Assist with training of new research assistants and coordinators;
    • Assist with scheduling and planning for visit capacity for assigned studies;
    • May set up, train and maintain all technology needed for studies;
    • May assist with study recruitment, patient enrollment, and tracking as needed;
    • May handle more complex study assignments and volumes;
    • May participate in community outreach / education events;
    • Maintaining confidentiality of patients, customers and company information, and;
    • Performing all other duties as requested or assigned.

    Minimum Qualifications

    A Medical Assistant diploma, LPN/LVN, EMT credential AND 2 years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.

    Required Skills

    • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
    • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
    • Strong organizational skills and attention to detail.
    • Well-developed written and verbal communication skills.
    • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
    • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
    • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
    • Must possess a high degree of integrity and dependability.
    • Ability to work under minimal supervision, identify problems and implement solutions.
    • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

    Benefits

    • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
    • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
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PRN Clinical Research Coordinator
  • Alcanza Clinical Research
  • Lakeland, FL PART_TIME
  • Department: OperationsEmployment Type: Part TimeLocation: Accel Research Sites - Lakeland, FLReporting To: Colleen FigueroaDescriptionAlcanza is a growing multi-site, multi-phase clinical research com...
  • Just Posted
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Clinical Trial Recruiter
  • Elixia Clinical Research Collaborative
  • , FL FULL_TIME
  • The Clinical Trial Recruiter assists and takes direction from the Recruitment Coordinator to identify patients who may qualify for clinical research trials conducted by the Company, in partnership wit...
  • 1 Day Ago
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Clinical Research Site Manager
  • Alcanza Clinical Research
  • Clermont, FL FULL_TIME
  • Department: OperationsEmployment Type: Full TimeLocation: Vertex Clinical Research | Clermont FLReporting To: Hayley MolinDescriptionAlcanza is a growing multi-site, multi-phase clinical research comp...
  • 9 Days Ago
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Licensed Clinical Social Worker
  • Pioneer Clinical Lab
  • The Villages, FL FULL_TIME
  • Premier Medical AssociatesLicensed Clinical Social WorkerThe Licensed Clinical Social Worker (LCSW) for Premier Medical Associates is a key member of the Primary Care Team, providing clinical services...
  • 11 Days Ago
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Clinical Research Coordinator
  • Ideal Clinical Research Inc
  • Miami, FL FULL_TIME
  • Company Description Ideal Clinical Research Inc is a clinical research organization located in Miami, FL. We take great pride in serving our sponsors with more than 4 South Florida locations. We condu...
  • 14 Days Ago
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Clinical Ethicist jobs at Popular Companies

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Medical Monitor - Clinical Research (Medical Degrees Only)
  • Piper Companies
  • Silver Spring, MD
  • Piper Companies (Health & Sciences) is seeking motivated candidates for aMedical Monitor and/or Safety & Pharmacovigilan...
  • 6/2/2024 12:00:00 AM
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Administrative Assistant
  • United Network For Organ Sharing
  • Richmond, VA
  • About the Position Position Description The Administrative Assistant provides high-level confidential administrative sup...
  • 6/2/2024 12:00:00 AM
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Pool Clinical Ethicist
  • The Tampa General Hospital Foundation Inc
  • Tampa, FL
  • Job Summary A Clinical Ethicist, also known as a Bioethicist, is a professional who advises on ethical and moral implica...
  • 6/1/2024 12:00:00 AM
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Clinical Ethicist
  • HH MedStar Health Inc.
  • Washington, DC
  • General Summary of Position Staff member of the John J. Lynch Center for Ethics sharing primary responsibility for the J...
  • 5/30/2024 12:00:00 AM
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Senior Analytics Engineer
  • United Network for Organ Sharing
  • Richmond, VA
  • About the Position Position Description The Senior Analytics Engineer will provide data management and engineering suppo...
  • 5/30/2024 12:00:00 AM
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Director, Cancer Biology
  • Sage Bionetworks
  • Seattle, WA
  • At Sage Bionetworks, we believe that we can learn more by engaging and collaborating with people from a diversity of exp...
  • 5/30/2024 12:00:00 AM
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Clinical Ethicist
  • Cleveland Clinic
  • Cleveland, OH
  • Cleveland Clinic's Center for Bioethics has an open position for a clinical ethicist whose primary responsibilities will...
  • 5/29/2024 12:00:00 AM
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Chaplain
  • Carle Health
  • Peoria, IL
  • Position Summary: Members of the Spiritual Care Team provide emotional/spiritual care, crisis intervention, conflict man...
  • 5/29/2024 12:00:00 AM
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About Florida

Florida (/ˈflɒrɪdə/ (listen); Spanish for "land of flowers") is the southernmost contiguous state in the United States. The state is bordered to the west by the Gulf of Mexico, to the northwest by Alabama, to the north by Georgia, to the east by the Atlantic Ocean, and to the south by the Straits of Florida. Florida is the 22nd-most extensive (65,755 sq mi or 170,300 km2), the 3rd-most populous (21,312,211 inhabitants), and the 8th-most densely populated (384.3/sq mi or 148.4/km2) of the U.S. states. Jacksonville is the most populous municipality in the state and the largest city by area in th...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Ethicist jobs
$95,246 to $119,644

Most Popular Cities in Florida for Clinical Ethicist Jobs

What does a Clinical Ethicist do?

Clinical Ethicist in Clearwater, FL
Those hired as full-time clinical ethicists brought a good deal of theoretical knowledge, but were unlikely to be immersed in the culture and norms of clinical medicine.
January 07, 2020
Clinical Ethicist in Charlotte, NC
Typically, they hold a PhD or at least a Master’s in medical ethics or a related discipline, and have some experience of working in a clinical environment.
February 19, 2020
Clinical Ethicist in Portland, ME
Bertino is a Clinical Ethicist at WellStar Health System in Atlanta, Ga.
December 21, 2019