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Clinical Research Coordinator
Clinical Research CoordinatorFlourish Research • Murrieta, California, USA
Clinical Research Coordinator

Clinical Research Coordinator

Flourish Research • Murrieta, California, USA
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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 Clinical Research Coordinators at our Murrieta site location. This is one of our three oncology research sites in the Greater Los Angeles area. These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network!

The Clinical Research Coordinator assists the Investigators in executing Phase I II III and IV clinical research trials in accordance with Standard Operating Procedures (SOPs) FDA and GCP guidelines and study protocols while providing an impeccable patient experience in every single interaction.

Shift : Monday-Friday 8 : 30 AM - 5 PM (occasional weekends)

Location : 25405 Hancock Ave Suite 110 Murrieta CA 92562

Compensation : $72000 - $79000 ($34.60 - $37.98 / hr)

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

  • Execute protocol-specified patient visits and procedures which may include but not limited to phlebotomy IVs injections vital signs ECG / EKG etc.
  • Document assessments and study data per regs / GCP; maintain complete source; accurately complete CRFs / eCRFs.
  • Obtain informed consent per federal regs GCP and IRB requirements.
  • Ethically recruit qualified subjects to meet enrollment timelines.
  • Complete required / ongoing training; attend investigator meetings / courses; stay current with changing regulations and Flourish policies.
  • Schedule and conduct visits per protocol timelines.
  • Protect confidentiality per HIPAA and all confidentiality agreements.
  • Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI / Sub-I / supervisor.
  • Account for and ensure availability of trial materials (study drug labs CRFs supplies).
  • Maintain and document communication with Leads Managers PIs / Sub-Is and study team per protocol and policy.
  • Perform duties safely and in a time- / cost-effective manner compliant with Flourish policies.
  • Represent Flourish professionally in all interactions.
  • Additional duties as assigned by management.

QUALIFICATIONS

  • Bachelors degree preferred but not required
  • Must have oncology clinical research experience
  • Minimum of two years of clinical research experience
  • Clinical skills highly preferred : vital signs EKG / ECG phlebotomy and injections
  • Familiar with e-source reporting via an electronic platform
  • A clear understanding of ICH FDA and GCP regulations
  • Impeccable organizational skills and attention to detail
  • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator research team Study Sponsor / CROs potential subjects and referral sources
  • An ethical compass that compels the candidate to be honest detail-oriented and self-driven
  • High-level critical thinking skills
  • Working knowledge of medical terminology and lab collection / processing / storage procedures
  • Proficiency with computers and Microsoft Office Suite
  • 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

    Yearly Salary Salary : 72000 - 79000

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    Clinical Research Coordinator • Murrieta, California, USA

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