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Company: DirectEmployers
Location: Aurora, CO
Career Level: Mid-Senior Level
Industries: Recruitment Agency, Staffing, Job Board

Description

Clinical Research RN (Open Rank) - 34387 University Staff

**Description**

**University of Colorado Anschutz Medical Campus**

**Department: Cancer Center**

**Working Title: Clinical Research RN (Open Rank)**

**Position #: 748446 - Requisition #: 34387**

**Job Summary:**

**Clinical Research Nurse (RN)**

**Examples of Work Performed by the Clinical Research Nurse (all levels)**

Assures adherence to all research standards as set forth by the Food and Drug Administration (FDA), the Office for Human Research Protections (OHRP), University of Colorado Hospital, University of Colorado Denver (UCD), National Cancer Institute (NCI) and other pertinent regulatory agencies.

Relays timely information to Regulatory Affairs Coordinator in regard to protocols (e. g. addition of investigators, amendments, serious adverse events, consent form changes, monitoring visits, correspondence, continuing review and study termination reports) to ensure quality study flow and ensure that all governing regulations are being adhered to.

Obtains medical history and current medications, reviews protocol inclusion/exclusion criteria, and confirms eligibility of subject. Ensures that the informed consent process has occurred, is properly documented and filed as required.

Recruits and interviews prospective subjects for multiple clinical studies. Familiarizes potential subjects with the details of the study through phone contacts and personal interviews.

Schedules subject participation in research, coordinating availability of necessary space, laboratory and physician support. Coordinates with pharmacy staff dispensing of study medication under the direction of the Principal Investigator and/or Sub-investigators.

Assures compliance with protocol details, completes necessary records, and coordinates scheduling of subject and monitoring visits. Accurately transfers source documentation into Case Report Form (CRF) within 10 working days. Is familiar with all records required for each study, reviews records after each visit for completeness and accuracy. Maintains patient clinical research files.

Submits and/or manages treatment plans through the UCHealth Beacon process and works with assigned staff for completion of the treatment plan.

Recognizes adverse events and serious events and promptly notifies appropriate parties; e. g. Principal Investigator, Study Sponsor, FDA, Data Safety and Monitoring Committee (DSMC), Regulatory Affairs Coordinator.

Serves as a contact person for ongoing clinical research studies and meets with representatives from sponsoring pharmaceutical firms or in-house staff for initial orientation to studies and for review of study records.

Participates in DSMC audits.

**Patient Care Responsibilities**

Collaborates with hospital staff to ensure tests and procedures required by clinical protocols are performed and documented. These include, but are not limited to vital signs, phlebotomy, specimen processing, EKG's, drug administration, Infusions, pharmacokinetic sampling, toxicity checks, and protocol specific tests and procedures.

May be called upon to perform the following specific tests and procedures specifically related to the research study: a) consenting, b) electrocardiogram, c)blood pressure, pulse, height, weight, pulse oximetry, and temperature measurements, d)phlebotomy and specimen processing and shipping

Collaborates with the clinical team in developing all aspects of patient care.

Assesses patient's pertinent health history.

Develops protocol specific source documents (e. g. data collection tools, study visit checklists, pharmacokinetic sample collection worksheets).

Assists team manager and/or financial team by processing bills and/or answering billing questions related to procedure performed for subjects enrolled to clinical trials.

Rotates through department PK (blood draw) schedule as necessary

Develop and review trial specific treatment (protocol)orders for accuracy and completeness prior to implementation in electronic medical record

**Examples of Work Performed by Clinical Research Nurse (Level II)**

Serves as primary coordinator for clinical trials

May be called upon for other department specific RN duties as needed

Teach, precept, and mentor new employees, as directed by team manager

Develop policy, procedure, patient education materials, and/or study tools as they relate to conduct of clinical research

**Examples of Work Performed by Clinical Research Nurse (Level III)**

Serves on internal CCTO committee

May be called upon for other department specific RN duties as needed

Teach, precept, and mentor new employees, as directed by team manager

**Work Location:**

Onsite

**Why Join Us:**

**Why work for the University?**

Medical: Multiple plan options

Dental: Multiple plan options

Additional Insurance: Disability, Life, Vision

Retirement 401(a) Plan: Employer contributes 10% of your gross pay

Paid Time Off: Accruals over the year

Vacation Days: 22/year (maximum accrual 352 hours)

Sick Days: 15/year (unlimited maximum accrual)

Holiday Days: 10/year

Tuition Benefit: Employees have access to this benefit on all CU campuses

ECO Pass: Reduced rate RTD Bus and light rail service

**Diversity and Equity:**

**Qualifications:**

**Minimum Qualifications:**

**Clinical Research Nurse - RN I Level (Intermediate)**

A bachelor's degree in biological sciences, nutrition, nursing, health, human services, social sciences or a directly related field from an accredited institution

RN License required (Current state nursing license or RN license from a participating state in the National Licensure Compact)

One (1) year of RN experience

**Clinical Research Nurse - RN II Level (Intermediate)**

A bachelor's degree in biological sciences, nutrition, nursing, health, human services, social sciences or a directly related field from an accredited institution

RN License required (Current state nursing license or RN license from a participating state in the National Licensure Compact)

Two (2) years of medical/surgical or oncology nursing experience, which must include at least one (1) year of clinical research experience.

**Clinical Research Nurse - RN III Level (Senior)**

A bachelor's degree in biological sciences, nutrition, nursing, health, human services, social sciences or a directly related field from an accredited institution

RN License required (Current state nursing license or RN license from a participating state in the National Licensure Compact)

Three (3)

Compensation Information:
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