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Flourish Research

Clinical trial optimization and operations efficiency

Research Concierge

Clinical Research OperationsPosted on Nov 9
Full-timeDetroit, MI, USA$24 - $35

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • At least 2 years of experience in a patient-facing healthcare, community health, or clinical research setting is required.
  • Communicate complex medical or research information clearly and compassionately to lay audiences.
  • Be comfortable using electronic health record systems and digital scheduling tools.
  • Maintain strong organization and accurate documentation, including current patient tracking logs.
  • Handle Protected Health Information discreetly and comply with HIPAA.
  • Communicate with patients in a patient-centered manner, adapting messages to their literacy and comfort level.
  • Self-direct schedule review and outreach proactively.
  • Navigate workflows across two separate organizations professionally.
  • Handle Protected Health Information with discipline and maintain patient and physician trust.
  • Explain trial participation basics, eligibility concepts, and patient rights clearly.

Responsibilities

  • Review partner-practice clinic schedules at least weekly before physician clinic days to identify patients who may qualify for active or upcoming trials.
  • Use electronic health record crawlers to identify qualifying diagnoses, medications, laboratory results, and demographics in the partner practice patient database.
  • Prepare a prioritized candidate list for physicians before each clinic day, flagged by study and qualification rationale.
  • Maintain and update a tracking log of patients identified, approached, and converted.
  • Receive physician warm handoffs to potential study candidates.
  • Conduct brief, non-coercive study conversations with interested patients in a private setting within the partner practice.
  • Walk interested patients to the research site for a facility tour or extended discussion when appropriate.
  • Present research participation as a positive, patient-centered opportunity rather than a sales transaction.
  • Document patient interactions and dispositions in Salesforce.
  • Facilitate limited prescreening for interested patients, including measuring blood pressure, point-of-care testing, capturing medication history, and brief eligibility screening.
  • Assist patients in completing informed consent for prescreening visits where applicable.
  • Schedule formal prescreening or screening visits at the research site in coordination with research coordinators.
  • Communicate screening outcomes and patient disposition to recruitment and clinical teams.
  • Educate patients about clinical research, how trials work, and what participation involves.
  • Distribute site-approved educational materials in partner-practice waiting areas and exam rooms.
  • Address patient concerns about time commitment, safety, compensation, and the differences between research and standard care.
  • Build awareness of the research site across the partner-practice patient population, including patients not flagged for a specific trial.
  • Contribute to developing and refining patient-facing educational content with the Site Director and research team.
  • Build and maintain ongoing relationships with partner-practice clinical staff, medical assistants, and front desk personnel to facilitate referrals.
  • Serve as an accessible point of contact for patients with questions about research participation.
  • Stay informed about active protocols at the research site to accurately explain study requirements and patient commitments.
  • Represent the organization professionally and courteously when interacting with staff, clients, and vendors.
  • Perform additional duties as assigned by management.

Desired Qualifications

  • Clinical background or certification as a Medical Assistant, Certified Nursing Assistant, Clinical Research Coordinator, or Licensed Practical Nurse.
  • Prior experience in patient navigation, community health outreach, or clinical trial recruitment.
  • Familiarity with the partner practice’s patient populations and therapeutic areas.
  • Experience with electronic medical record data mining or patient panel management.
  • Bilingual skills based on local community demographics.
  • A valid driver’s license may be beneficial for occasional off-site outreach activities.

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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