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Clinical Research Coordinator
Clinical Research CoordinatorFlourish Research • Inverness, Colorado, USA
Clinical Research Coordinator

Clinical Research Coordinator

Flourish Research • Inverness, Colorado, USA
1 day ago
Job type
  • Full-time
Job description

Flourish Research is looking for motivated talented creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package a supportive and collaborative work environment and endless growth opportunities.

We are actively hiring a Clinical Research Coordinator at our Inverness research site location.

The Clinical Research Coordinator (CRC) is responsible for the ethical and accurate coordination and administration of clinical trials under the direction of the Site Manager the Principal Investigator and the Medical Director. The CRC will perform diverse administrative and clinical duties requiring analysis sound judgement and a high level of knowledge of study-specific protocols while providing an impeccable patient experience in every single interaction.

Shift : Monday-Friday 7 AM - 4 PM (occasional weekends)

Location : 411 West Highland Boulevard Inverness FL 34452

Compensation : Hourly rate based on experience

Benefits : Health dental and vision insurance plans 401(k) with 4% match tuition reimbursement parental leave referral program employee assistance program life insurance disability insurance and 15 days of PTO 10 company holidays.

RESPONSIBILITIES

  • Maintain familiarity with FDA regulations for clinical research
  • Administratively and clinically manage approximately six to ten clinical trials
  • Adhere to company Standard Operating Procedures Good Clinical Practice and study protocols
  • Ensure scientific integrity of data and protect the rights safety and well-being of patients enrolled in clinical trials
  • Obtain Informed Consent from study participants and verify documentation
  • Screen potential study participants for inclusion / exclusion criteria
  • Schedule and conduct study visits per protocol requirements including but not limited to the following :

Dispense study medication in a professional and accountable manner

  • Collect process and ship blood / urine specimens
  • Perform ECGs obtain vital signs
  • Administer questionnaires / diaries
  • Complete source documentation and maintain timely completion of case report forms
  • Ensure prompt reporting of events to sponsor and IRB
  • Assess participants condition and report any significant variations from baseline measurements to Principal Investigator
  • Submit timely patient reimbursement requests to financial team for patients participation in protocol
  • Ensure the filing and maintenance of all regulatory documents
  • Schedule and prepare for monitoring visits
  • Maintain communication with Principal Investigator Sub Investigators Assistants sponsors IRB
  • Other duties as assigned by management
  • QUALIFICATIONS

  • Bachelors degree preferred
  • Associates degree in nursing or related field preferred
  • Two years in a related healthcare position
  • Pleasant outgoing and mature. Good communication and time management skills. Attention to detail. Self-disciplined and motivated. Diligent and persistent.
  • High level of integrity and accountability
  • Abiility to function effetively and positively in a team environment
  • Must have the ability to establish and maintain good working rapport with study patients physicians investigators referring physicians research staff and clinic
  • Must exhibit accurate complete legible and timely use of communication methods
  • Familiar with medical terminology
  • BCLS training required
  • Recommended to sit for Certified Clinical Research Coordinator certification after two years experience
  • Flourish Research offers an excellent comprehensive benefits package a supportive and collaborative work environment and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

    Flourish Research is where clinical trials thrive.

    Flourish Research represents one of the industrys most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology / metabolic disorders / renal CNS pulmonology and vaccines.

    At Flourish Research we strive toward clinical trials and healthcare excellence means everyone deserves the best care regardless of their race color gender identity religion ethnicity physical abilities age sexual orientation or veteran status. We embrace employees customers and patients from these underrepresented groups to help make this vision a reality.

    Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees customers and patients are included and treated with dignity and respect.

    Flourish Research strives to build an organization that attracts and leverages diversity in our staff which reflects the diversity of our local communities. We promote education acceptance and inclusion because there is beauty in diversity. The more diversity we have in our team the more unique perspectives and ideas we share and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

    It is the policy of Flourish Research not to discriminate against any applicant for employment or any employee because of age color sex disability national origin race religion or veteran status.

    Required Experience :

    Senior IC

    Key Skills

    CSS,Cloud Computing,Health Education,Actuary,Building Electrician

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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    Clinical Research Coordinator • Inverness, Colorado, USA

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