Nurse Practitioner Sub-Investigator TX

BioTalent; San Antonio (TX); On-site; USD 110,000 - 140,000; Full time

Job summary

BioTalent is seeking a Nurse Practitioner to join our clinical research team as an NP Sub-Investigator for Phase I–IV trials. You will support the Principal Investigator, perform medical assessments, and oversee study visits within regulatory requirements.

Qualified candidates hold an active NP license and have clinical research experience, with strong communication and collaboration skills. Travel may be required; US work authorization is mandatory.

Qualifications

• Active NP license (US) required.
• Clinical research experience preferred.
• Knowledge of GCP/ICH and IRB regulations.
• Industry-sponsored trial experience preferred.

Responsibilities

• Serve as Sub-Investigator supporting the Principal Investigator in clinical trials.
• Conduct medical assessments and study visits.
• Evaluate participant eligibility and monitor treatment response.
• Assess and manage adverse events.
• Ensure compliance with study protocols and regulatory requirements.
• Collaborate with CRAs, sponsors, monitors, and IRBs.
• Support informed consent and trial documentation.
• Participate in investigator meetings, monitoring visits, and audits.
• Assist with patient recruitment and coordinating with referring providers.

Skills

Communication skills

Presentation skills

Collaboration

Patient assessment

Independent decision making

Education

NP license

Job description

Are you a Nurse Practitioner with clinical research experience and an interest in helping advance new therapies?

We’re looking for an NP Sub-Investigator to join a clinical research team supporting Phase I–IV clinical trials.

What You’ll Do

• Serve as a Sub-Investigator, supporting the Principal Investigator in clinical trials
• Conduct medical assessments and study visits
• Evaluate participant eligibility and monitor treatment response
• Assess and manage adverse events
• Ensure compliance with study protocols, GCP/ICH, and regulatory requirements
• Work closely with Clinical Research Coordinators, sponsors, monitors, and IRBs
• Support informed consent and clinical trial documentation
• Participate in investigator meetings, monitoring visits, and audits
• Help support patient recruitment and relationships with referring providers
• Active/current NP license
• Clinical experience with strong patient assessment skills
• Knowledge of GCP, ICH, IRB, and clinical research regulations
• Previous Sub-Investigator experience in industry-sponsored clinical trials preferred
• Strong communication, presentation, and collaboration skills
• Comfortable working independently and making clinical decisions within protocol and regulatory requirements
• Willingness to travel overnight when needed

Work Authorization:

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time

If you're an NP looking to combine clinical practice with clinical research and investigator responsibilities, we'd love to connect!