Part-Time PRN Research Nurse Practitioner

Tranquil Clinical and Research Consulting Services LLC; Texas; On-site; USD 62,000 - 90,000; Part time

Job summary

Tranquil Clinical and Research Consulting Services LLC is seeking a Part Time Research Nurse Practitioner PRN to ensure patient safety and coordinate study visits. The role operates in an office-based setting alongside the principal investigator, with responsibilities spanning protocol adherence, subject screening, and study initiation activities.

The ideal candidate holds a Nurse Practitioner credential with clinical trial experience, strong knowledge of FDA regulations and GCP, and excellent

Qualifications

• NP with related clinical experience
• Experience working on clinical trials for a minimum of 1 year
• Knowledge of FDA regulations and GCP
• Accuracy, attention to detail and ability to set priorities and meet deadlines
• Basic Computer Skills required: Microsoft Office Suite, including Word PowerPoint, Excel
• Excellent bedside manner and patient-centric focus
• Excellent time management and social skills
• Highly motivated with a phenomenal eye for detail

Responsibilities

• Coordinate and perform study visits under the supervision of the PI
• Develop management systems and prepare for study initiation
• Screen and enroll study subjects per protocol
• Manage study-related activities, subject compliance, and documentation
• Attend study-related meetings and communicate effectively with the team
• Ensure informed consent is signed and adherence to protocol guidelines

Skills

Clinical trial experience

Nurse Practitioner

FDA regulations & GCP knowledge

Attention to detail

Time management

Team collaboration

Microsoft Office Suite

Tools

Microsoft Office Suite

Job description

Tranquil Clinical and Research Consulting Services LLC is seeking a Part Time Research Nurse Practitioner PRN to ensure patient safety and coordinate study visits. The role operates in an office-based setting alongside the principal investigator, with responsibilities spanning protocol adherence, subject screening, and study initiation activities.

The ideal candidate holds a Nurse Practitioner credential with clinical trial experience, strong knowledge of FDA regulations and GCP, and excellent