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Flourish Research

Clinical trial optimization and operations efficiency

New Patient Navigator

Clinical Support & Patient AdministrationUpdated on Nov 14
Full-timeWalnut Creek, CA, USA$35 - $43 /hr

About the Job

Requirements

  • A bachelor's degree or equivalent experience is required.
  • At least five years of experience working directly with patients, including referral coordination, patient navigation, or managing relationships with physician offices.
  • Proven organizational skills and strong attention to detail are required.
  • Strong time-management, communication, presentation, and interpersonal skills, both written and oral, are required.
  • Ability to build trusted working relationships with physicians, office staff, and internal teams, and maintain those relationships through consistent follow-through, is required.
  • Excellent computer skills, including Office 365 products, are required.
  • Ability to work independently and professionally with urgency and self-motivation is required.
  • Ability to collaborate and align with operations is required.
  • Demonstrated decision-making, critical-thinking, and problem-solving abilities are required.
  • Project-management skills to handle competing priorities and meet deadlines are required.
  • Understanding of clinical research processes is required.
  • Knowledge of HIPAA and patient privacy requirements is required.

Responsibilities

  • Serve as the main administrative contact for referring physicians and their office staff for referrals, questions, and patient status.
  • Promptly acknowledge incoming referrals to referring offices and confirm what is needed to move each patient forward, including records, imaging, pathology, and insurance information.
  • Update referring physicians at each milestone, including consult scheduling, screening, enrollment, or screen failure; when a trial is not a fit, coordinate the patient's return to the referring physician's care.
  • Schedule calls or meetings between referring physicians and Valkyrie Principal Investigators or the Medical Director when clinical questions arise.
  • Maintain an up-to-date referral source directory with practice contacts, preferred communication methods, referral volume, and practice-specific records or order requirements.
  • Onboard referring practices after a partnership is established by the Site Director or Medical Director by setting up referral workflows, sharing forms and records requirements, and confirming contacts on both sides.
  • Keep referring offices current on open trials and slot availability using site-approved materials, and coordinate logistics for office visits, lunch-and-learns, and community events led by Site leadership.
  • Support community partnerships with organizations serving diverse populations by managing contact lists, scheduling, and outreach materials.
  • Log physician and community partner interactions and flag relationship concerns, including slow responses, missed updates, or declining referral volume, to the Site Director.
  • Contact new patients within established referral turnaround times and keep patients and families informed from referral intake through Cycle 1 Day 1.
  • Schedule and coordinate initial new patient consult visits, matching each patient to the appropriate provider based on diagnosis and open trials.
  • Collect and upload medical records before consults, including pathology, imaging, labs, treatment history, and biomarker results, and flag gaps to the clinical team before they cause delays.
  • Learn each patient's diagnosis, stage, and treatment history sufficiently to recognize missing, inconsistent, or clinically significant information and promptly escalate it to the Principal Investigator or clinical team.
  • Address logistical barriers for patients and families, including transportation, lodging, travel, parking, and appointment conflicts, using site and sponsor resources, and ensure each patient has a next step.
  • Assist with scheduling during the screening period in coordination with the assigned Clinical Research Coordinator.
  • Complete a documented handoff to the assigned Clinical Research Coordinator at Cycle 1 Day 1, covering collected records, consent and screening status, insurance authorization status, open logistics, and patient and family preferences.
  • Become proficient in using the Electronic Medical Record and Clinical Trial Management System to enter and manage patient information accurately.
  • Work closely with Principal Investigators and the Clinical Research Team to ensure slot availability and match potential patients for screening.
  • Track referrals and referral sources, including time from referral to consult and consult to enrollment, and use the data to provide regular updates to referring physicians and practice partners.
  • Support the generation and review of periodic reports for Site and Medical Directors.
  • Adapt to additional responsibilities as required by organizational needs and leadership.
  • Represent Flourish Research professionally and courteously, verbally, in writing, and in appearance, when interacting with staff, clients, and vendors.
  • Perform additional duties as assigned by management.

Desired Qualifications

  • Prior oncology experience and exposure to clinical research are preferred.
  • Working knowledge of medical terminology and oncology medical records, including pathology reports, imaging, and treatment history, is preferred.

About the Company

Flourish Research

Clinical trial optimization and operations efficiency

Flourish Research helps healthcare and pharmaceutical clients run clinical trials more efficiently. It offers tailored optimization services that improve trial operations, aiming to reduce time and costs to bring new treatments to market. The company leverages decades of experience to provide quality-driven solutions, focusing on expanding capabilities, developing healthy teams, and implementing processes that enhance speed and quality across trial activities. Flourish Research differentiates itself by its client-specific approaches and strong emphasis on quality, team development, and operational excellence to deliver reliable trial outcomes.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Apex, NC
Founded
2021

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