Sub Investigator, NP/PA-C

Hawthorne Health

Nurse Practitioner or Physician Assistant leading clinical trials at a community-based research site. Ensuring adherence to protocols and participant safety in Conroe, TX.

Posted 6/29/2026contractConroe • Texas • 🇺🇸 United StatesMid-LevelSenior💰 $150 per hourWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Assist the Principal Investigator (PI) in overseeing and managing clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
Provide medical oversight and ensure the safety and well-being of study participants throughout the trial, under the supervision of the PI.
Perform delegated study-related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings.
Review and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision.
Assist the PI in making medical decisions regarding participant care, adverse events, and protocol deviations.
Ensure accurate, complete, and timely collection and documentation of all study data.
Communicate effectively with the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
Assist with investigational product accountability, storage, and administration according to protocol.
Participate in site initiation visits, monitoring visits, audits, and inspections as required.
Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas.

Requirements

What you’ll need

Must be a NP or PA-C able to work with adult and pediatric patients.
Experience working on at least 3 sponsor initiated clinical trials as a Sub Investigator.
Demonstrated knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
Strong interpersonal and communication skills, with the ability to work effectively as part of a team.
Excellent clinical judgment and problem-solving abilities.
Meticulous attention to detail and strong organizational skills.
Ability to prioritize tasks and manage time efficiently.
Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus.
Commitment to ethical conduct and patient safety.

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Hawthorne Health Website LinkedIn All Job Openings 1 - 10 employees Founded 2000 We pride ourselves on offering both our clients and our candidates a very high level of personal service underpinned by an ongoing commitment to quality, integrity and affordability, we are a recruitment agency you can trust. Sub Investigator, NP/PA-C Job not on LinkedIn 🔥 17 minutes ago 🏢🏡 Conroe – Hybrid 💵 $150 / hour ⏳ Contract/Temporary 🟡 Mid-level 🟠 Senior ✨ Investigator Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Assist the Principal Investigator (PI) in overseeing and managing clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
Provide medical oversight and ensure the safety and well-being of study participants throughout the trial, under the supervision of the PI.
Perform delegated study-related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings.
Review and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision.
Assist the PI in making medical decisions regarding participant care, adverse events, and protocol deviations.
Ensure accurate, complete, and timely collection and documentation of all study data.
Communicate effectively with the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
Assist with investigational product accountability, storage, and administration according to protocol.
Participate in site initiation visits, monitoring visits, audits, and inspections as required.
Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas. 🎯 Requirements
Must be a NP or PA-C able to work with adult and pediatric patients.
Experience working on at least 3 sponsor initiated clinical trials as a Sub Investigator.
Demonstrated knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
Strong interpersonal and communication skills, with the ability to work effectively as part of a team.
Excellent clinical judgment and problem-solving abilities.
Meticulous attention to detail and strong organizational skills.
Ability to prioritize tasks and manage time efficiently.
Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus.
Commitment to ethical conduct and patient safety. Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

Clinical Trial OversightPatient AssessmentsEligibility ScreeningsData DocumentationAdverse Event Management

Soft Skills

Problem-SolvingAttention To DetailOrganizational SkillsTime ManagementTeam Collaboration

Certifications

NP CertificationPA-C Certification