Research Clinician

Element Materials Technology

Centennial, COFull-timePosted Apr 5, 2026

25–45 an hour

Behavioral Health Market Context

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Job Description

nsure that the studies meet requirements of the Quality System.

$25 - $45/hr doe
Responsibilities
• Responsible for clinical care of participants, according to protocol requirements and/or Element standing orders. Develops, completes, and maintains source documents.
• Screens, consents, and conducts study procedures as designated by the study protocol.
• Adheres to study protocol and follows participants through the study period, per protocol.
• Conducts required assessments throughout the clinical trial assessment period.
• Responsible for maintaining and completing case report forms in agreement with the source documentation and in accordance with the study protocols.
• Assures clinical supply accountability for assigned trials.
• Accompanies sponsor representatives during site visits and follows up as needed.
• Accumulates all data and supplies for study closure.
• Performs procedures (e.g., vital signs, laboratory tests, etc.) as required by the protocol and as allowed by level of licensure and/or training.
Skills / Qualifications
• Must be a Registered Nurse or Registered Respiratory Therapist with a current license in the state of Colorado, or a degree and licensing required.
• Must not have any disciplinary action on license history.
• Clinical research experience preferred, but not required.
• Must be capable of performing all clinical tasks relevant to licensure and/or training.
• Must be able to clearly communicate (verbal and written) and interface with participants.
• Must have good interpersonal skills, demonstrated through interactions with participants, Element staff, Sponsor representatives, etc.
• Must be detail-oriented and organized.
• Proficiency in Microsoft applications (Word, Excel, PowerPoint, Outlook).
• Availability, flexibility, and maturity to represent the company at a broad range of events/projects in the community, with customers and within the company.
• Well-developed oral and written communication skills to meet a variety of communication needs, good interpersonal skills that foster open upward and downward communication built on mutual respect.
• Possession of independent problem‑solving abilities.
• Knowledge and compliance with laboratory procedures, quality and safety requirements.
• Strong organizational and scheduling skills.
• Technical background is a plus.
Company Overview

Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to “Make tomorrow safer than today”.

When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.

While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development.

Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization.
Diversity Statement

At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our vision of becoming “the world’s most trusted testing partner”.

All suitably qualified candidates will receive consideration for employment on the basis of objective work-related criteria and without regard for the…

Qualifications

  • Must be a Registered Nurse or Registered Respiratory Therapist with a current license in the state of Colorado, or a degree and licensing required
  • Must not have any disciplinary action on license history
  • Must be capable of performing all clinical tasks relevant to licensure and/or training
  • Must be able to clearly communicate (verbal and written) and interface with participants
  • Must have good interpersonal skills, demonstrated through interactions with participants, Element staff, Sponsor representatives, etc
  • Must be detail-oriented and organized
  • Proficiency in Microsoft applications (Word, Excel, PowerPoint, Outlook)
  • Availability, flexibility, and maturity to represent the company at a broad range of events/projects in the community, with customers and within the company
  • Well-developed oral and written communication skills to meet a variety of communication needs, good interpersonal skills that foster open upward and downward communication built on mutual respect
  • Possession of independent problem‑solving abilities
  • Knowledge and compliance with laboratory procedures, quality and safety requirements
  • Strong organizational and scheduling skills

Benefits

  • $25 - $45/hr doe

Responsibilities

  • The main responsibility of the Research Clinician is to assist the Clinical Study Manager in facilitating the study in each laboratory in order to meet customer turnaround time and requests; to help ensure the studies are performed to protocol(s) requirements; to ensure that the studies meet requirements of the Quality System
  • Responsible for clinical care of participants, according to protocol requirements and/or Element standing orders
  • Develops, completes, and maintains source documents
  • Screens, consents, and conducts study procedures as designated by the study protocol
  • Adheres to study protocol and follows participants through the study period, per protocol
  • Conducts required assessments throughout the clinical trial assessment period
  • Responsible for maintaining and completing case report forms in agreement with the source documentation and in accordance with the study protocols
  • Assures clinical supply accountability for assigned trials
  • Accompanies sponsor representatives during site visits and follows up as needed
  • Accumulates all data and supplies for study closure
  • Performs procedures (e.g., vital signs, laboratory tests, etc.)
  • as required by the protocol and as allowed by level of licensure and/or training


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