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Sub-Investigator (Nurse Practitioner / Physician Assistant)
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#702246
Full Time
Job Description
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
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
