Onsite NP/PA Sub-Investigator - IV Infusion Expert

M3USA; Los Angeles (CA); On-site; USD 68,880 - 96,432; Part time

Job summary

M3 Wake Research in Encino, CA is seeking a Part-Time Sub-Investigator (NP/PA) to join our clinical trials team. The role focuses on conducting study visits, collecting data, and ensuring protocol compliance under the supervision of the PI or Medical Director.

The ideal candidate has a Master's degree, NP/PA licensure, and at least 2 years of clinical research experience, with phlebotomy and IV/infusion experience. Familiarity with FDA regulations, ICH-GCP, and ISO standards is preferred.

Qualifications

• Master's Degree required.
• Licensed Nurse Practitioner/Physician Assistant.
• At least 2 years of clinical research or sub-investigator experience preferred.
• Phlebotomy training required.
• IV and infusion experience required.
• FDA regulations, ICH-GCP and ISO knowledge.
• Strong teamwork and communication skills.
• Ability to multi-task and work with interdisciplinary teams.

Responsibilities

• Reviews, comprehends, and adheres to assigned study protocol.
• Assists trial investigators in screening and review of potential study participants' eligibility.
• Conducts subject visits.
• Maintains case report forms, patient charts and documentation.
• Ensures that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Collects and enters data as necessary.
• Reviews lab results, imaging reports, and other study-specific reports.
• Completes required protocol training

Skills

Nurse Practitioner/PA role

Clinical research experience

Phlebotomy

IV/infusion experience

FDA/ICH-GCP knowledge

Teamwork

Communication skills

multitasking and independent work

Education

Master's Degree

Job description

M3 Wake Research in Encino, CA is seeking a Part-Time Sub-Investigator (NP/PA) to join our clinical trials team. The role focuses on conducting study visits, collecting data, and ensuring protocol compliance under the supervision of the PI or Medical Director.

The ideal candidate has a Master's degree, NP/PA licensure, and at least 2 years of clinical research experience, with phlebotomy and IV/infusion experience. Familiarity with FDA regulations, ICH-GCP, and ISO standards is preferred.