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Profound Research

Clinical trial site network for community physicians

Assistant Clinical Research Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCarlsbad, CA, USANo salary listed

About the Job

Requirements

  • A bachelor's degree and 1 year of relevant life-science industry experience, or an associate's degree and 2 years of relevant experience, or a high school or technical degree and at least 3 years of relevant experience.
  • Demonstrated knowledge of medical terminology.
  • Ability to use computers, Microsoft Office software, fax machines, copiers, and multi-line telephones.
  • Experience performing clinical assessments such as obtaining vital signs, conducting electrocardiograms, drawing blood, and processing or shipping laboratory specimens.

Responsibilities

  • Work under the direction of clinical research site management, the Principal Investigator, and senior clinical research staff.
  • Participate in active patient recruitment efforts.
  • Support the lead clinical research coordinator and clinical research staff with daily trial activities, including phlebotomy, laboratory work, data entry, and administrative assignments.
  • Conduct assigned clinical-trial activities in accordance with research protocols and standards and applicable laws, regulations, policies, and procedures.
  • Complete required training, including International Council for Harmonisation Good Clinical Practice certification and International Air Transport Association certification, in a timely manner.
  • Coordinate assigned trial duties under supervision, including study start-up, vendor management, subject recruitment, source-document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, adverse-event and serious adverse-event management and reporting, deviation management and reporting, and monitoring visits and follow-up.
  • Apply good documentation practices when collecting, maintaining, and correcting study data and required clinical-trial records, including source documentation, case report forms, queries, drug-dispensation records, and regulatory forms.
  • Communicate professionally with coworkers, leadership, study subjects, sponsors, contract research organizations, and vendors.
  • Collect and account for sponsor-provided supplies, including laboratory kits, ancillary supplies, and investigational products.
  • Understand key timelines, endpoints, required vendors, and patient populations for each assigned protocol.
  • Perform other duties as assigned.

About the Company

Profound Research

Clinical trial site network for community physicians

Profound Research is a clinical research organization that operates a nationwide network of trial sites, partnering with community physicians to bring pharmaceutical and biotech studies into everyday medical practices. It recruits and enrolls patients from a combined database of more than 1.25 million people, coordinates site operations and investigator oversight, and runs studies across more than 15 therapeutic areas on behalf of trial sponsors. Its network spans 22 sites across four geographies, with over 1,000 providers, 110-plus active investigators, and more than 130 clinical trials conducted to date. What sets Profound Research apart is its model of embedding research infrastructure within existing community practices, giving physicians and their patients access to experimental treatments without leaving their local care setting. The goal is to expand patient access to new treatments while helping sponsors conduct trials through a community-based site network.

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