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Clinical Research Coordinator, Georgetown TX

Company: Care Access
Location: Georgetown
Posted on: September 24, 2022

Job Description:

We are SO glad you are reading this! But, before we go any further in this conversation, we have deal-breakers. You must meet all of the following criteria before applying:

You MUST have a minimum of 3 years of experience as a Clinical Research Coordinator.

You must have experience checking and documenting vitals and EKG (ECG) in the past year.

Must have Phlebotomy skills and experience.

You must have the authorization to work in the US for any employer.

You must not need visa sponsorship, either now or in the future.

We are glad you are still reading.

Care Access is seeking a dedicated, experienced, and innovation-driven Clinical Research Coordinator to help us with coordinating several studies at our site located in Georgetown, TX. You will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required at the location.

On a day-to-day basis you will:

  • Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelines
  • Coordinating the operational aspects of a new and ongoing clinical trial at the site
  • Working under the supervision of the Principal Investigator(s), while exercising excellent clinical judgment in patient monitoring and care
  • Maintaining daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general daily communication
  • Responsibility for the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol
  • Patient recruitment and pre-screening
  • Maintaining and submitting IRB communications and regulatory documents
  • Timely communications with internal teams, investigators, review boards, and study subjects
  • Preparing other study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs and drug/device accountability logs
  • Willingness for some travel, as it is a requirement for this position
  • Other duties as assigned

    To be successful in this role, you will bring:
    • The position requires at least a High School Diploma
    • At least Three (3) years of experience as a Clinical Research Coordinator is required
    • Must have Investigational New Drug (IND) or Investigational Product (IP) clinical trial experience.
    • Ability to check and document vitals as well as EKG (ECG)
    • Phlebotomy experience is a plus
    • Good management and organizational skills, understanding of medical procedures
    • Exceptional interpersonal skills, the ability to work independently
    • Ability to lift a minimum of 50 pounds
    • Command of professional and Business English (written and spoken)

      Benefits offered:
      • PTO/Vacation days, sick days, Holidays.
      • 100% paid Medical, Dental and Vision Insurance. 50% for dependents.
      • HSA plan
      • Short-term disability, long-term disability, Life Insurance.
      • Continued Education Allowance
      • Culture of growth and equality
      • 401K plan and matching contribution

        About us

        At Care Access, every day we are advancing medical breakthroughs. We're uniting standard patient care with cutting-edge treatments and research. The work that we do brings life-changing therapies to those who are in need and paves the way for newer and greater treatments to reach the world. We're proud to advance these breakthroughs and to work with the big players while also engaging with the very best physicians and caring for patients. Through innovation and a unique technology-enabled service model, our team of experts is paving the way to take this vision forward.

        We care. Our values are rooted in being genuine, finding new ideas, and building something meaningful. Influenced by our values, we have built a culture valuing communication and dialogue: we care about what everyone has to say and we spend energy on being equal and inclusive. Along the way, we are caring for each other, accelerating medicine, and seeding a long-term impact for generations to come.

        We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

        By applying to this post, you agree to receive text message updates about your application and interview process.

Keywords: Care Access, Georgetown , Clinical Research Coordinator, Georgetown TX, Healthcare , Georgetown, Texas

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