Research Clinician

Benefits

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
• •9 more items(s)

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
• •9 more items(s)