Clinical Research Nurse II performs a full range of clinical and non-clinical research duties, and has a working knowledge of the clinical research process and the regulations that govern it. As licensed professionals with clinical research experience, they perform patient related care independently, including medical assessments, symptom management, and referrals, within the scope of their licensure. With the oversight of the PI or their designee, they perform progressively more complex and comprehensive clinical research duties at an ever-increasing level of independence, working closely with the Principal Investigator (PI). They work under supervision, but with more autonomy than an entry level position.
**SIGN ON BONUS ELIGIBLE $15,000**
This is available to external hires only, for full time 40 hour positions only and certain conditions apply.
Responsibilities
Responsibilities:
a. Utilize electronic systems, technologies, and software necessary for study operations.
b. Accurately document study visit assessments for data collection and trains others to these standards.
c. Assist with data entry as needed.
d. Contribute to the development of data collection documents and instruments.
e. Detect issues related to data capture, collection or management; suggest solutions.
f. Investigate incomplete or inaccuate documents to ensure completeness of data.
g. Assist with development of SOPs for data quality assurance.
h. Adhere to processes and run queries, summaries, and report to monitor the quality of data.
i. Utilizes required processes, policies, and systems to ensure data security.
4. Leadership and Professionalism
a. Adheres to professional guidelines and code of ethics related to the conduct of clinical research.
b. Mentor and train new and current clinical research staff in departmental research and administrative procedures
c. Support efforts to maintain an adequate number of competent staff to conduct clinical research in complaince with all regulartory, institutional and departmental requirements.
5. Site and Study Management
a. May support site selection, feasibility, and study start up proccesses
b. Assist in the initiation, management, and completion of clinical trials and research studies.
c. Encourage standardization of processes and procedures.
d. Implement a plan to ensure a safe, clean, and secure enviroment of care for patients, visitors, and staff
e. Perform other dutys as assigned, such as supporting regulatory affairs.
6. Communication and Team Science
a. Collaborate with and educate healthcare professionals regarding investigational research protocols
b. Ensure research compliance and adherence to protocol guidelines.
7. Portfolio and Program Development & Management
a. May participate in committees or working groups to strenghten research implementation and practice.
8. Clinical Skills
a. Ensure a safe, effective, and efficient patient care environment
b. Facilitate and monitor activities related to the deliver of patient care within research
9. Perform other duties as assigned.
Qualifications
Required Licensure/Certifications
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