Clinical Research Director jobs in Saint Petersburg, FL

Clinical Research Director directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Clinical Research Director ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Additionally, Clinical Research Director typically reports to top management. The Clinical Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be a Clinical Research Director typically requires 5+ years of managerial experience. (Copyright 2024 Salary.com)

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Research Assistant
  • Alcanza Clinical Research
  • Largo, FL FULL_TIME
  • Research Assistant

    Department: Operations

    Employment Type: Full Time

    Location: Accel Research Sites - Largo, FL

    Description

    Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in Boston and Northern MA, Portsmouth, NH, Charleston, SC, Charlotteville, VA, and Detroit, MI. 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 Research Assistant (RA) will perform administrative tasks as needed for the successful operation of the clinical research site.


    Key Responsibilities

    Responsibilities may include but are not limited to:

    • Assists with the basic screening of patients for study enrollment;
    • Assists with patient follow-up visits;
    • Documents in source clinic charts;
    • Enters data in EDC and answers queries;
    • Request and track medical record requests;
    • Enters data in EDC and answers queries;
    • Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and
    • Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;
    • Ensures study-related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
    • Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;
    • Maintains strict confidentiality of patients, employees, customers, and company information at all times and adheres to HIPAA Guidelines; and
    • Perform all other duties as requested or assigned.


    Skills, Knowledge and Expertise

    Minimum Qualifications: An Associate’s degree OR a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. 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).
    • Must possess 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 hire. 
    • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, and supplemental insurance are offered.
    • A 401k plan with an employer safe harbor match is also offered, with enrollment eligibility being the first of the month following 30 days of employment.
  • 1 Month Ago

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RN Clinical Research Nurse
  • Johns Hopkins Medicine
  • Petersburg, FL FULL_TIME
  • Work Hours Monday- Friday 7:30am-4:00pm (hours are flexible) Location: ST Petersburg, Florida Johns Hopkins All Children's Hospital (JHACH) is a premiere clinical and academic health system, providing...
  • Just Posted

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Clinical Research Coordinator I
  • Johns Hopkins Medicine
  • Petersburg, FL FULL_TIME
  • Johns Hopkins All Children's Hospital is a premiere clinical and academic health system, providing expert pediatric care for infants, children and teens with some of the most challenging medical probl...
  • 3 Days Ago

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Clinical Research Coordinator II
  • Johns Hopkins Medicine
  • Petersburg, FL FULL_TIME
  • Come be a part of something bigger and work with the #1 Children's Hospital in Florida! We are Magnet designated & ranked nationally in 8 specialties by US News & World Report for 2021-2022! Clinical ...
  • 8 Days Ago

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Research Coordinator Clinical I
  • Johns Hopkins Medicine
  • Petersburg, FL FULL_TIME
  • Elevate your possibilities! • Career growth and development • Diverse and collaborative working environment • Affordable and comprehensive benefits package Johns Hopkins All Children's Hospital is a p...
  • 27 Days Ago

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Clinical Research Coordinator - Pediatric Orthopaedic Surgery
  • CHILDREN'S ORTHOPAEDIC AND SCOLIOSIS SURGERY ASSOC
  • Petersburg, FL FULL_TIME
  • We are currently seeking a Clinical Research Coordinator to join our team! The Clinical Research Coordinator is responsible for providing advanced level research support. They will be responsible for ...
  • 1 Month Ago

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0 Clinical Research Director jobs found in Saint Petersburg, FL area

St. Petersburg is a city in Pinellas County, Florida, United States. As of the 2015 census estimate, the population was 257,083, making it the fifth-most populous city in Florida and the largest in the state that is not a county seat (the city of Clearwater is the seat of Pinellas County). St. Petersburg is the second-largest city in the Tampa Bay Area, after Tampa. Together with Clearwater, these cities comprise the Tampa–St. Petersburg–Clearwater Metropolitan Statistical Area, the second-largest in Florida with a population of around 2.8 million. St. Petersburg is located on the Pinellas pen...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Director jobs
$135,427 to $182,819
Saint Petersburg, Florida area prices
were up 1.1% from a year ago

Clinical Research Director in Killeen, TX
We are Looking for an Assistant Director for the Center for Clinical Research Education.
December 07, 2019
Clinical Research Director in Springfield, IL
During the Clinical Research Operations Forum a few weeks ago, Stephen Sonstein, Ph.D., Professor & Program Director for Clinical Research Administration at Eastern Michigan University spoke on the shift in clinical research going from a focus on regulatory compliance to a standardization of competencies for professionals working in the field.
February 06, 2020
Clinical Research Director in Olympia, WA
You might occasionally be able to enter from the administration side - for example, you could start as a study-site coordinator in the NHS or as a clinical trials administrator.
January 28, 2020