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Flourish Research

Clinical trial optimization and operations efficiency

Clinical Research Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timePlymouth Meeting, PA, USA$25 - $36 /hr

About the Job

Requirements

  • Must have oncology clinical research experience.
  • Must have a minimum of two years of clinical research experience.
  • Clinical skills in vital signs, electrocardiography, phlebotomy, and injections are highly preferred.
  • Must be familiar with electronic source reporting via an electronic platform.
  • Must have a clear understanding of International Council for Harmonisation, Food and Drug Administration, and Good Clinical Practice regulations.
  • Must have working knowledge of medical terminology and laboratory collection, processing, and storage procedures.
  • Must be proficient with computers and Microsoft Office Suite.
  • Must have strong organizational skills and attention to detail.
  • Must have communication and interpersonal skills to interact effectively with the Principal Investigator, research team, study sponsors and contract research organizations, potential subjects, and referral sources.
  • Must have ethical judgment, honesty, attention to detail, and self-direction.
  • Must have critical-thinking skills.

Responsibilities

  • Execute protocol-specified patient visits and procedures, including phlebotomy, intravenous procedures, injections, vital signs, and electrocardiograms.
  • Document assessments and study data according to regulations and Good Clinical Practice, maintain complete source documentation, and accurately complete case report forms and electronic case report forms.
  • Obtain informed consent according to federal regulations, Good Clinical Practice, and Institutional Review Board requirements.
  • Ethically recruit qualified subjects to meet enrollment timelines.
  • Complete required and ongoing training, attend investigator meetings and courses, and stay current with changing regulations and company policies.
  • Schedule and conduct visits according to protocol timelines.
  • Protect confidentiality according to the Health Insurance Portability and Accountability Act and confidentiality agreements.
  • Report adverse events promptly; report serious adverse events to the sponsor within 24 hours and notify the Principal Investigator, Sub-Investigator, or supervisor.
  • Account for and ensure the availability of trial materials, including study drugs, laboratory materials, case report forms, and supplies.
  • Maintain and document communication with leads, managers, Principal Investigators, Sub-Investigators, and the study team according to protocol and policy.
  • Perform duties safely and in a time- and cost-effective manner in compliance with company policies.
  • Represent the company professionally in all interactions.
  • Perform additional duties as assigned by management.

Desired Qualifications

  • A bachelor's degree is preferred but not required.

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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