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Sub-Investigator (Nurse Practitioner / Physician Assistant)

Biopharma Informatic, Houston, TX, United States



Job Description:
Biopharma Informatic is a fast-growing clinical research organization dedicated to advancing innovative therapies through high-quality clinical trials. We partner with sponsors and investigators to deliver efficient, patient-centered research across a variety of therapeutic areas.

We are seeking a highly motivated Sub-Investigator (Nurse Practitioner or Physician Assistant) to support the Principal Investigator in the execution of clinical trials. This role is ideal for a provider with strong clinical judgment, attention to detail, and an interest in research. This will also be a hybrid position and candidate must have reliable transportation as they may need to travel to different locations in the Houston and Katy area.

Key Responsibilities:
Serve as a Sub-Investigator on clinical trials under the direction of the Principal Investigator
Conduct study visits, including physical exams, medical assessments, and protocol-required procedures
Evaluate and document adverse events (AEs/SAEs) and ensure timely reporting
Assess subject eligibility in compliance with regulatory requirements
Review laboratory results, diagnostic tests, and study data for clinical significance
Ensure protocol adherence and compliance with FDA and ICH-GCP guidelines
Collaborate with study coordinators, sponsors, and cross-functional teams
Support audit readiness and participate in monitoring visits and regulatory inspections
Maintain accurate and timely source documentation

Qualifications:
Licensed Nurse Practitioner (NP) or Physician Assistant (PA)
Active DEA license (preferred)
Minimum 1–2 years of clinical experience (research experience preferred but not required)
Strong understanding of clinical research processes and regulatory standards is a plus
Excellent communication, organizational, and critical thinking skills
Ability to work in a fast-paced, collaborative environment

Preferred Experience:
Prior experience in clinical trials (phases I–IV)
Experience in relevant therapeutic areas (IV infusions, rheumatology experience)
Familiarity with EDC systems and EMR platforms

Requirements added by the job poster
• Authorized to work in the United States
• No need for visa sponsorship