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Science 37

Virtual site platform for decentralized trials

Neurologist Consultant

Physicians & SurgeonsPosted on Nov 13
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • An advanced degree in Medicine (MD or equivalent) is required.
  • Board certification in Neurology is required.
  • Experience as a Principal Investigator, focused on pharmaceutical-sponsored studies, is required.
  • Expertise in project management, including the ability to lead and manage research personnel, solve problems proactively, and follow through, is required.
  • Knowledge of field organizational strategies and the ability to adapt to a rapidly changing work environment, manage decentralized teams, and make responsive decisions are required.
  • Extensive knowledge of clinical research, including the drug development process and critical elements for successful clinical trials, is required. The role requires participation in and contribution to trial activities, the ability to create and review protocols and programs, and the ability to assess project feasibility and pathways to success.
  • Strong written and verbal communication and presentation skills are required, including the ability to maintain positive relationships with sponsors, project team members, and internal colleagues, and to conduct effective presentations.
  • Working knowledge of Google applications and the ability to generate business correspondence, create forms, and generate reports are required.
  • The ability to communicate in English, verbally and in writing, is required.

Responsibilities

  • Function as the Principal Investigator for clinical trials when Science 37 conducts a study as a Direct to Patient trial.
  • Function as a Sub-Investigator for clinical trials in therapeutic areas or indications aligned with the physician’s clinical expertise and experience.
  • Coordinate with the Site Operations Manager to identify, onboard, and train investigators for Science 37 studies.
  • Educate and train the Science 37 study team about the target patient population and treatment paradigms for indications in Science 37 studies.
  • Collaborate with a Business Development counterpart to review study opportunity synopses and protocols and assess their fit and feasibility for the decentralized trial model.
  • Support a Business Development counterpart during sponsor and client meetings and teleconferences.
  • Serve as a subject matter expert to support Science 37 study opportunities and develop study opportunity proposals.
  • Collaborate with the Science 37 Regulatory Affairs team to engage the FDA and other global regulatory bodies regarding the decentralized trial model.
  • Work with sponsors and collaborators to identify clinical endpoints suitable for decentralized clinical trial conduct.
  • Collaborate with sponsors and regulatory bodies to migrate endpoints from clinic-based conduct and validate their use for in-home conduct.
  • Represent Science 37’s expertise in decentralized clinical trials and the relevant therapeutic area at industry and clinical conferences and webinars.
  • Publish peer-reviewed articles and white papers related to therapeutic-area expertise and the decentralized clinical trial model.

Desired Qualifications

  • Knowledge of Spanish is preferred.

About the Company

Science 37

Virtual site platform for decentralized trials

Science 37 runs a clinical research platform focused on decentralized (site-less) trials, offering technology and services to pharma, biotech, and CROs, centered on its Metasite platform and remote patient recruitment. Its Metasite virtual site connects patients at home with telemedicine physicians, mobile nurses, and coordinators for remote visits, data capture, and eConsent, with Metasite Rescue available to accelerate enrollment and standardized workflows to improve data quality and diversity. The company differentiates itself by providing a single unifying, site-less platform that enables fully remote participation and removes geographic barriers, integrating telemedicine, remote monitoring, and digital consent. Its goal is to make clinical trials more accessible and efficient by expanding patient access, boosting enrollment diversity, and delivering faster, higher-quality trial data using a unified digital trial platform.

Company size
201-500
Company stage
IPO
Headquarters
Morrisville, NC
Founded
2014

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