Quality Control Investigator Jobs in Baton Rouge, LA

The Clinical Research Nurse - RN, under the guidance and supervision of the Principal Investigator (PI), ensures that the integrity and quality of clinical trials are maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals and FMOLHS policies and procedures. The research nurse will coordinate, manage, and assist physicians in enrolling, assessing and monitoring patients on Industry-Sponsored, NCI-Sponsored and/or Investigator Initiated clinical trials offered.
 

Experience:
Two years as a Clinical Registered Nurse (Bachelor's degree may be substituted for one year of work experience). One year of clinical research experience preferred.

Education:
BSN or RN

Special Skills:
Detail Oriented
Ability to proactively identify and solve problems
Strong communication skills with patients, physicians, and team members
Professional demeanor
Ability to work independently and in a team environment
Strong interpersonal, customer service and multi-tasking skills
Proficiency in Microsoft Office Word and Excel, Electronic Health Systems, and databases and/or have a willingness to learn and demonstrate proficiency within six months of hire
Work well under pressure and manage deadlines
 

Licensure
Current, unencumbered Registered Nurse license in the state of Louisiana

1.   
Providing Nursing Care to Research Study Participants
Participates in recruitment and selection of study participants in conjunction with treating physician by conducting a thorough review of participant's medical history
Informs, educates, and consents clinical research patients regarding clinical trial participation, potential investigational treatment plan and general study participant requirements
Ensures compliance with study protocols by providing thorough patient assessment and documentation at each study visit
Performs procedures according to study protocols (including, but not limited to venipuncture, EKG, study Investigational Product (IP) administration)
Collection, processing, storage, and shipment of patient specimens (blood, sputum, tissue, etc. as directed by study protocols)
Submission of appropriate reports as required by IRB, Sponsor, or any research entity
Working in collaboration with research pharmacist(s) to ensure proper inventory of IP is maintained at all times
Disburses IP and provides patient teaching regarding IP administration as necessary
Communicates and collaborates with study team including internal and external parties, sponsors, PI, and study participants
2.   
Quality
Ensures site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for research activities
Provides accurate and timely data collection, documentation, entry and reporting in Sponsor's electronic data capture systems
Ensures compliance with research protocols, by providing ongoing quality control audits
Maintains current training including Good Clinical Practice, IATA/Dangerous Goods Handling, and study specific training as required by sponsors
Utilizes all equipment, supplies, facilities, and resources in a prudent and efficient manner to ensure efficient departmental operations and the provision of high-quality health care services
Promotes the quality and efficiency of his/her own performance by remaining current with the latest trends in field of expertise through participation in job-relevant seminars and workshops, attendance at professional conferences, and affiliations with national and state professional organizations
3.   
Collaboration and Partnership
Manages relationships with study sponsors, investigators, and associated staff to provide the highest level of performance
Collaborate and meet in person and virtually with study monitors/auditors to ensure study data quality
Attends and participates in committees, meetings and programs as required to meet requirements/standards of FMOLHS accreditation organizations
Works to develop the clinical research department by marketing the services of the department to physicians conducting research within FMOLHS and in the private practice setting
Maintains communication with administrative staff for pertinent research opportunities that may become problematic for FMOLHS structures (standards, ERDs, policies and procedures, etc.)