Gas Controller

Element Materials TechnologyBoulder County, CO
12d$40 - $60

About The Position

Element has a current opening for a Gas Controller to join our growing team in Boulder, CO for full time position. The main responsibility of the Gas Controller is to support invasive and non-invasive hypoxia clinical trials ensuring compliance with protocols and regulatory standards. Position will work alongside the Clinical Study team focusing on study execution, monitoring participant safety, and using necessary equipment to desaturate participants to target clinical trial levels. $40hr-$60hr DOE

Requirements

  • Candidates for consideration will include Engineers with Clinical experience, Registered Nurse, or Respiratory Therapist with a current license
  • Must be capable of performing all clinical tasks relevant to licensure and/or training
  • Must be able to clearly communicate verbally with participants
  • Must have good interpersonal skills, demonstrated through interactions with participants, 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
  • Ability to interface with participants
  • Possession of good communication skills (verbal, written)
  • Possession of independent, problem-solving abilities
  • Knowledge and compliance with laboratory procedures, quality and safety requirements
  • Strong Organizational and Scheduling Skills

Nice To Haves

  • Familiarity with pulse oximetry, oxygen levels
  • Biomedical engineering experience
  • Clinical Research Experience and Good Clinical Practices
  • Systems engineering experience and ability to tie requirements to outcomes.

Responsibilities

  • Performs procedures as required by the protocol and as allowed by level of licensure and/or training.
  • Comfortable working with gases under high pressure.
  • Follow proper procedures for moving tanks, disconnecting / reconnecting pressure regulators, understanding Primary, secondary pressure regulation, open close valves.
  • Technical troubleshooting capabilities with gas controlling equipment and interfaces
  • Responsible for care of clinical trial participants, according to protocol requirements and/or standing orders.
  • Comfortable reading graphs (xy plots, bar, etc.) along with digital values and determining responses needed for data.
  • Develops, completes, and maintains source documents
  • Adheres to study protocol and follows participants through the study period, per protocol
  • Conduct 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
  • Accompanies sponsors representatives during site visits and follows up, as needed
  • Assess what data has been collected, and what needs to be collected for individual study participants on the fly.
  • Additionally quick assessment of combined data set and what needs to be collected in upcoming participants during the study.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Education Level

No Education Listed

Number of Employees

5,001-10,000 employees

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