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  • Clinical Research Nurse Coordinator

    Actalent (Orlando, FL)



    Apply Now

    Clinical Research Nurse Coordinator

     

    MUST HAVE a minimum of 2 years of Clinical Research experience

     

    Work under limited supervision to plan, coordinate, evaluate, and perform nursing care for research participants

     

    Collect data for assigned research projects, following study-specific protocol guidelines, and will communicate with Principal Investigators (PI),

     

    Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff

     

    Deliver safe care and demonstrate regard for the dignity and respect of all participants

     

    Maintain clinical competencies including physical assessment, phlebotomy, and IV insertion

     

    Practice the principles of Universal Precautions and adhere to HIPAA regulations

     

    Maintain a clean and prepared clinical space, performing set-up and turnover procedures in all clinical areas as per SOPs

     

    Participate in internal and/or external training programs to maintain licensure

     

    Utilize positive interpersonal communication skills, effectively communicating with healthcare team members, patients, investigators, sponsors of research, and

     

    administration

     

    Review all elements of the current institutional IRB-approved informed consent document with study candidates and/or their legal representatives, ensuring

     

    patient advocacy and informed consent as an ongoing process

     

    Manage multiple clinical trial protocols, coordinate their execution and follow-up, and ensure accurate, legible, and timely documentation

     

    Manage records, study medication, and test articles in a confidential and secure manner

     

    Promote PI oversight by advising the PI, sub-investigator(s), Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and

     

    issues relevant to the integrity of the trial and/or safety of research subjects

     

    Coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols

    Qualifications

    MUST HAVE a minimum of 2 years of Clinical Research experience

     

    Associate degree in Nursing

     

    Active State of Florida Registered Nurse license

     

    BLS certification

     

    Ability to perform clinical tasks, including assisting physicians and CRNs with minor procedures and other study requirements within the scope of practice

     

    Ability to acclimate and integrate into various clinical settings as needed per protocol

     

    Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs

    Pay and Benefits

    The pay range for this position is $74880.00 - $98000.00/yr.

     

    Benefits from Day One

     

    Paid Days Off from Day One

     

    Career Development

     

    Whole Person Wellbeing Resources

     

    Mental Health Resources and Support

     

    Pet Insurance*

     

    Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

     

    Workplace Type

     

    This is a fully onsite position in Orlando,FL.

     

    Application Deadline

     

    This position is anticipated to close on May 23, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

     


    Apply Now



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