Sub-Investigator / Nurse Practitioner

BioTalent; San Antonio (TX); On-site; USD 100,000 - 150,000; Full time

Benefits offered by this job

Medical and dental benefits

401(k) with company match

Paid time off

Job summary

BioTalent in San Antonio is seeking an experienced Nurse Practitioner to serve as a Sub-Investigator at our clinical research site. You will work with the Principal Investigator and team to oversee medical care of trial participants and ensure studies are conducted safely, accurately, and in compliance with protocols and regulatory requirements. This role supports Phase I–IV studies and collaboration on innovative therapies and professional growth within a collaborative research environment.

Qualifications

• Licensed NP in Texas and valid TX license.
• Previous Sub-Investigator experience on industry-sponsored trials preferred.
• Clinical research experience required or preferred.
• Solid knowledge of GCP, ICH guidelines, FDA regulations, and trial protocols.
• Excellent communication and teamwork skills.
• Willingness to travel overnight as needed.

Responsibilities

• Provide clinical oversight as Sub-Investigator for study participants.
• Conduct medical assessments, visits, and procedures per protocol.
• Evaluate eligibility based on protocol criteria.
• Monitor participant safety and report adverse events.
• Ensure informed consent is properly obtained.
• Maintain study documentation and regulatory compliance.
• Collaborate with PI, coordinators, sponsors, monitors, and team.
• Review documentation for data accuracy and consistency.
• Support compliance with GCP, ICH, FDA requirements, and study protocols.
• Participate in sponsor meetings, monitoring visits, audits, and investigator meetings.
• Assist with study feasibility and provide clinical input for new trials.
• Support patient recruitment and retention efforts.
• Oversee handling of investigational products as applicable.
• Maintain current credentials and regulatory documentation.

Skills

Nurse Practitioner license

Clinical research

GCP & ICH knowledge

FDA regulations familiarity

Strong communication

Team collaboration

Travel readiness

Education

Nurse Practitioner license (TX)

Tools

Microsoft Word

Microsoft Excel

Clinical research systems

Job description

We are seeking an experienced Nurse Practitioner to serve as a Sub-Investigator at a clinical research site in San Antonio. This individual will work closely with the Principal Investigator and research team to oversee the medical care of clinical trial participants and ensure studies are conducted safely, accurately, and in compliance with study protocols and regulatory requirements.

This is an opportunity to play an important role in Phase I–IV clinical research, working alongside an experienced research team and contributing to the development of new and innovative therapies.

Key Responsibilities

• Serve as a Sub-Investigator and provide clinical oversight for study participants.
• Conduct study-related medical assessments, office visits, and clinical procedures in accordance with study protocols.
• Evaluate participant eligibility based on protocol inclusion and exclusion criteria.
• Assess participant response to treatment and monitor overall safety throughout the study.
• Evaluate, document, and appropriately report adverse events and serious adverse events.
• Ensure informed consent is properly obtained and documented before study procedures are performed.
• Maintain a thorough understanding of assigned study protocols, investigational products, and regulatory requirements.
• Work closely with the Principal Investigator, research coordinators, sponsors, monitors, and other members of the research team.
• Review study documentation and ensure clinical data is accurate, complete, and consistent with source records.
• Support compliance with Good Clinical Practice (GCP), ICH guidelines, FDA requirements, IRB requirements, and study protocols.
• Participate in sponsor meetings, monitoring visits, audits, and investigator meetings as needed.
• Assist with study feasibility and provide clinical input regarding potential new trials.
• Support patient recruitment and retention efforts, including collaboration with physicians and other healthcare providers.
• Ensure appropriate handling, use, and oversight of investigational products when applicable.
• Maintain required regulatory documentation and current professional credentials.
• Support the overall quality and successful execution of clinical trials at the site.

Qualifications

• Licensed Nurse Practitioner (NP) required.
• Current and unrestricted license to practice in Texas.
• Previous experience serving as a Sub-Investigator on industry-sponsored clinical trials strongly preferred.
• Clinical research experience highly preferred.
• Strong understanding of GCP, ICH guidelines, FDA regulations, and clinical trial protocols.
• Knowledge of medical terminology and clinical documentation.
• Ability to independently assess participants and make appropriate clinical decisions within protocol and regulatory requirements.
• Strong communication and interpersonal skills with the ability to collaborate effectively with patients, research staff, sponsors, and healthcare providers.
• Highly organized with strong attention to detail and documentation.
• Comfortable working in a fast-paced clinical research environment.
• Basic proficiency with Microsoft Word, Excel, and clinical research systems.
• Ability to travel overnight occasionally for investigator meetings or other business needs.

What’s Offered

• Competitive salary of $100,000–$150,000
• Medical and dental benefits
• 401(k) with company match
• Paid time off
• Opportunity to work on innovative clinical trials and contribute directly to the development of new therapies
• Collaborative clinical research environment with opportunities for continued professional growth