Research Clinician

Element Materials Technology•Boulder County, CO

16d•$25 - $45•Onsite

About The Position

Element has a current opening for a Research Clinician to join our growing team in Boulder County, CO on a full-time basis. 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 turn 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. $25-$45/hr. DOE

Requirements

Must be a Registered Nurse or Registered Respiratory Therapist with a current license in the state of Colorado/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

Nice To Haves

Clinical Research Experience preferred, but not required
Technical background is a plus

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
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
Assures clinical supply accountability for assigned trials
Accompanies sponsors representatives during site visits and follows up, as needed
Accumulates all data and supplies for study closure
Performs procedures (i.e. vital signs, laboratory tests, etc.), as required by the protocol and as allowed by level of licensure and/or training