• Clinic Lab Technician I

    Teva Pharmaceuticals (Miramar, FL)
    …Screen, COVID-19 testing, etc.) and processes in strict compliance with the study protocol, Good Clinical Practice (GCP) standards, Standard Operating Procedures ... for ensuring timely, accurate, and comprehensive processing during screening, admission, study conduct, and discharge procedures. **How you'll spend your day**… more
    Teva Pharmaceuticals (12/12/25)
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  • Site Care Partner/Lead CRA - FSP

    Parexel (Tallahassee, FL)
    …Partner is a crucial liaison for investigative sites throughout a study 's lifecycle, responsible for site start-up, activation, relationship management, recruitment, ... + Maintains a knowledge of assigned protocols + Conducts study start-up activities at the site level including but...for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness… more
    Parexel (11/22/25)
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  • Director, Oncology Scientific Communications

    Pfizer (Tampa, FL)
    …enrich the SCP (based on wide cross-functional input) with evolving evidence from clinical studies , insights, the Clinical Development Plan and regulatory ... + Chair Scientific Publications Committees (SPCs) + Work closely with clinical study teams during data readouts to determine publication content + Ensure… more
    Pfizer (12/13/25)
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  • Site Research Assistant

    IQVIA (Miami, FL)
    …consent forms, and study schedules. + Skill in carrying out required clinical procedures. + Working knowledge of medical terminology. + Ability to pay close ... This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of… more
    IQVIA (11/25/25)
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  • Senior Precision Medicine Associate- FSP

    Parexel (Tallahassee, FL)
    …of clinical trial samples + Provides support for sample related matters to clinical study teams + Works with Informed Consent Form (ICF) Specialist and ... clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** ** Study Team Support** +… more
    Parexel (11/08/25)
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  • Non-Registered Polysomnographic Technologist

    Cleveland Clinic (Weston, FL)
    …of Sleep Medicine, Cleveland Clinic's Sleep Disorders Center performs more than 9,000 sleep studies each year, using each result to help our patients find answers in ... Polysomnographic Trainees. + Review history/physical information, medications, test requests and study protocol. + Complete and verify all documentation (pre- and… more
    Cleveland Clinic (11/27/25)
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  • Summer Internship Program: Global Development…

    Takeda Pharmaceuticals (FL)
    …**Job Description** Global Development Compliance ensures quality and compliance in Clinical Development in partnership with R&D Quality and GCP Functions. We ... continuous improvement, foster innovation, and maintain an efficient, inspection-ready clinical development model. Embracing technology and automation, we aim to… more
    Takeda Pharmaceuticals (12/12/25)
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  • Medical Instrument Technician (Polysomnography)

    Veterans Affairs, Veterans Health Administration (Orlando, FL)
    …medical terminology and medical record organization to review medical records, sleep study orders, consent forms, and medical charts, etc. Knowledge of basic anatomy ... system for electroencephalography (EEG) monitoring in order to conduct the sleep study . Removes electrodes and sensors at completion of study . Knowledge… more
    Veterans Affairs, Veterans Health Administration (10/08/25)
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  • Data Management Lead

    Parexel (Tallahassee, FL)
    …in leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or Real World Data, with a good understanding of molecule and ... West Coast hours. **About Us:** At Parexel, we are dedicated to advancing clinical research and supporting medical affairs with innovative solutions. We are seeking… more
    Parexel (10/11/25)
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  • CRA 2, Cell & Gene Therapy, Car-T, Iqvia Biotech

    IQVIA (Tampa, FL)
    …trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, ... bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role… more
    IQVIA (12/02/25)
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