Clinical Operations Jobs in Kansas (NOW HIRING)

Job Title: Clinical Research Nurse I (Day Shift)

Job Description

The Clinical Research Nurse I plays a key role in ensuring the safety, comfort, and informed consent of clinical trial participants while supporting the successful execution of study protocols. This role involves performing a range of clinical trial procedures, maintaining safety equipment readiness, and serving as a resource and mentor to the Clinical Operations team. The position is based in a clinical research unit in the Overland Park, KS suburb and follows a Monday–Friday day shift schedule.

Responsibilities

• Ensure the safety and informed consent of clinical trial participants throughout the course of each study.
• Carry out clinical trial procedures in accordance with study protocols, Good Clinical Practice (GCP) guidelines, and Standard Operating Procedures (SOPs).
• Perform ongoing monitoring and safety evaluations for clinical trial participants.
• Administer investigational products (IP) as directed by study protocols.
• Perform catheter placement and other required clinical procedures within the scope of practice.
• Safeguard the privacy and confidentiality of all clinical trial participants and sponsor information at all times.
• Serve as a mentor and resource to members of the Clinical Operations team, offering guidance and support as needed.
• Identify opportunities to improve safety practices and communicate recommendations to department leadership.
• Observe, document, and ensure appropriate follow-up for any participant adverse events, in alignment with study and safety requirements.
• Coordinate Basic Life Support (BLS) and Advanced Life Support (ALS) training sessions for Clinical Operations staff, as needed.
• Promote and uphold high standards of customer service, quality, and patient safety within the department.
• Support study-related informed consent processes during participant screenings when required.
• Provide training to staff on clinical trial processes relevant to their roles and responsibilities.
• Communicate study updates and progress to appropriate team members to support effective collaboration.
• Proactively escalate issues related to participant safety, protocol adherence, or operational challenges and share potential solutions with supervisors and management.
• Assist with pre-screening patients for eligibility based on study criteria.
• Support patient recruitment activities for clinical trials.
• Conduct chart reviews to identify potential participants and to verify study-related information.

Essential Skills

• Active Registered Nurse (RN) license with eligibility to practice in Kansas.
• Ability to perform clinical procedures such as monitoring, safety evaluations, investigational product administration, and catheter placement within the RN scope of practice.
• Strong commitment to maintaining participant privacy and confidentiality.
• Ability to follow detailed study protocols, GCP guidelines, and SOPs with high attention to detail.
• Capability to observe, document, and follow up on adverse events accurately and promptly.
• Effective communication skills for interacting with participants, colleagues, and interdisciplinary teams.
• Ability to mentor and serve as a resource to Clinical Operations staff.
• Organizational skills to manage multiple study-related tasks and responsibilities.
• Basic Life Support (BLS) certification or ability to obtain and maintain BLS certification.
• Capacity to coordinate and support BLS and ALS training sessions for staff.
• Ability to work the specified day shift schedule (0600–1430, Monday–Friday).

Additional Skills & Qualifications

• No prior clinical research experience is required; training will be provided.
• Advanced Life Support (ALS) certification is not required; support is available to help recertify if needed.
• Experience with pre-screening patients and patient recruitment is beneficial.
• Familiarity with chart review processes is an advantage.
• Interest in clinical research and willingness to learn study-specific procedures and documentation requirements.
• Ability to contribute to a culture of high-quality patient care, safety, and customer service.

Work Environment

This position is based in a clinical research unit located in the suburb of Overland Park, KS. The role operates in a structured, protocol-driven environment focused on participant safety and high-quality clinical research. The standard schedule is Monday through Friday, 6:00am–2:30pn, providing consistent daytime hours. The nurse works closely with Clinical Operations staff and other research professionals, using standard clinical equipment and safety devices in accordance with GCP and SOPs. The environment emphasizes teamwork, continuous learning, and adherence to safety and quality standards, with appropriate clinical attire required to maintain a professional and hygienic setting.

This is a Contract position based out of Overland Park, KS.

The pay range for this position is $39.00 - $40.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Overland Park,KS.

This position is anticipated to close on Jul 27, 2026.

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