Enjoy what you do while contributing to a company that makes a difference in people’s lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do, building families, offers stimulation, challenge, and personal reward.

We are searching for a PRN Research Nurse for our Clear Lake, TX location.

Responsibilities include but are not limited to:

• Completes forms and generates all reports necessary to comply with regulatory requirements and institutional policies
• Works closely with the Research Director, clinical trial coordinators, research staff, and investigators to ensure that all regulatory documents for the research studies are up-to-date.
• Maintains a process to track each protocol through the submission and approval process
• Assists with investigational study selection and project negotiation, including initial site/sponsor correspondence.
• Assessment, planning, evaluation, and intervention for the well being of study patients.
• Provides quality clinical care and educates patients on the fertility process.
• Performs clinical activities and administrative work in support of the research study.
• Attends required study meetings and remains current on procedures & protocols.
• Develops standard study operation procedures for SGF Services LLC.
• Provides training tools and information for Nurses, Medical Assistants, Sonographers, and other clinical & administrative staff as needed.
• Creates and prepares study patient information packs.
• Schedules and conducts study consultations with patients.
• Obtains and maintains informed consents.
• Maintains study patient charts and documentation.
• Maintains study patient recruitment.
• Participates in medication administration.
• Occasionally performs routine patient assessment if needed (height, weight, vital signs, etc.).
• Assists physicians with procedures, exams as needed.
• Documents patient care services by charting in patient and department records including the EHR systems and Clinical Information System

What you'll bring:

• 3+ years of experience preferred managing and submitting regulatory documentation for clinical trials (IRB/GCP/FDA)
• Experience managing FDA clinical research trials
• Current RN license
• Ability to access, input, and retrieve information from a computer.
• Current CPR certification, or acquire within 1 month of employment.
• Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.).
• Ability to work as part of a multi disciplinary team and autonomously.
• Ability to communicate accurately and concisely; excellent interpersonal skills.
• Proven ability to meet deadlines and follow-through on projects.
• Ability to work independently to manage a caseload of patients.

What We Offer:

We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types:

• Full-Time Employees (30+ hours/week):
  Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays
• Part-Time Employees:
  401(k) with company match and performance-based bonus opportunities
• Per Diem Employees:
  401(k) with company match

To learn more about our company and culture, visit here.

How To Get Started:

To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.