Clinical Research Nurse - Cancer Center
Clinical Research Nurse - Cancer Center
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1 Vacancy
Job Description
Who is Saint Louis University Founded in 1818 Saint Louis University is one of the nations oldest and most prestigious Catholic universities. SLU which also has a campus in Madrid Spain is recognized for world-class academics life-changing research compassionate health care and a strong commitment to faith and service.
JOB SUMMARY
Under the direction of the Principal Investigator or designee the Clinical Research Nurse I is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs devices or research interventions. The Clinical Research Nurse I is a a member of the team and resource for study protocol conduct acting as a liaison between the SLU SOM clinical partners (ex. SSM Health) the Principal Investigator Institutional Review Board (IRB) and sponsors to ensure good clinical practice standards (GCP) throughout the life cycle of the study.
PRIMARY JOB RESPONSIBILITIES
Review and abstract medical record information and ensure proper adherence to randomization schema study drug dosing and administration.
Screen patients according to study criteria randomize enroll and obtain consent.
Administratively responsible for scheduling performing and/or supervising required study tests.
Perform nursing assessments of study participants.
Document and record in writing or electronically all study events and protocol related procedures.
Review clinical system billing charges for accuracy and appropriateness.
Ensure that all required study event(s) and protocol related data are accurately and efficiently entered in the clinical trial management system.
Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation protocol submissions and standard operating procedures (SOPs).
Enters and collects study related data and develops per appropriate processes. Ensures accuracy and completeness of data for all studies. Recognizes and reports security of physical and electronic data vulnerabilities.
Maintains participant-level documentation for all studies including those that are complex in nature require access to the EHR or require SLUCare/SSM charge routing. Screen participants for complex studies (e.g. procedural and interventional studies).
Conducts visits for complex studies (e.g. procedural and interventional studies).
Identifies all adverse events (AEs) and determines whether or not they are reportable. Collaborates with the PI to determine AE attributes including relatedness to study. Conducts and documents consent for participants for all types of studies including those that are complex in nature and/or require clinical research orders in EHR.
Performs other duties as assigned.
KNOWLEDGE SKILLS & ABILITIES
Proficiency in electronic medical records and relevant computer software.
Strong verbal and written communication skills and attention to detail is essential.
Ability to work in a team environment to facilitate the integrity of the study and its timely completion.
Ability to travel to off-site locations.
MINIMUM QUALIFICATIONS
RN with current registration to practice nursing in St. Louis.
3-5 years of relevant nursing experience.
Current BLS Certification
Can easily use computing software and web based applications (e.g. Microsoft Office products and the electronic medical record).
PREFERRED QUALIFICATIONS:
Clinical Research experience strongly preferred.
Function
Clinical ResearchScheduled Weekly Hours:
40Saint Louis University is an equal opportunity/affirmative action employer. All qualified candidates will receive consideration for the position applied for without regard to race color religion sex age national origin disability marital status sexual orientation military/veteran status gender identity or other non-merit factors. If accommodations are needed for completing the application and/or with the interviewing process please contact Human Resources at .
Employment Type
Full-Time
