Description

JOB DESCRIPTION

Responsible for planning, organizing, leading, and performing comprehensive advanced level clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the clinical trials. Performs patient related care and assessments independently and within the scope of their licensure. Participates in decisions regarding the clinical research process.

Principal Accountabilities:

1. Plans, coordinates and evaluates nursing care of participants for clinical research projects, following specific research study protocol guidelines.
2. Communicates and interacts with research investigators, sponsoring agencies and other parties involved in the coordination of research activities.
3. Assists in the compilation, analysis and documentation of findings.
4. Has specialized depth and/or breadth of expertise in own discipline or function.
5. Interprets internal or external issues and recommends solutions/best practices.
6. Solves complex problems and takes a broad perspective to identify solutions.
7. Works independently, with guidance in only the most complex situations.
8. Progression to this level is typically restricted on the basis of business requirement.
9. Performs other related duties as assigned.

QUALIFICATIONS

Minimum Education and/or Experience Requirements:

Education:

• Doctor of Philosophy (PhD) in Nursing or related research-focused discipline required; Doctor of Nursing Practice (DNP) with demonstrated research experience may be considered.
• Master of Science in Nursing (MSN) from an accredited institution required.
• Advanced coursework or certification in research design, data analysis, or evidence-based practice preferred.

Experience:

• Minimum of 5-7 years of clinical nursing experience required.
• Minimum of 3 years of experience in nursing or clinical research, including leadership of projects from conception through dissemination.
• Demonstrated success in mentoring staff or students in research and EBP.
• Prior experience managing IRB submissions, compliance documentation, and regulatory reporting required.
• Proven track record of peer-reviewed publications and/or grant-funded projects
• preferred.