Sub-Investigator Clinical Trials

Stamford Therapeutics Consortium is an established Phase II-IV clinical research site conducting industry-sponsored clinical trials across multiple therapeutic areas. We are seeking an experienced Nurse Practitioner (NP) or Physician Assistant (PA) to serve as a Sub-Investigator (Sub-I) on select studies.

ALSA Research is a privately owned and operated clinical research site network specializing in phase II, III, and IV clinical trials for the pharmaceutical and biotechnology industries. Founded in 1994, the company’s sole mission is to conduct the highest quality clinical trials so that new, safe and effective medications can be developed, researched and approved for a variety of indications and diseases.

Job Type & Hours

• Flexible schedule:typically 5–10 hours per week during busy enrollment periods; some weeks may be lighter

About the Opportunity

We are an established Phase II-IV clinical research site conducting industry-sponsored clinical trials across multiple therapeutic areas. We are seeking an experiencedNurse Practitioner (NP) or Physician Assistant (PA)to serve as aSub-Investigator (Sub-I)on select studies.

This role is perfect for a clinician who wants topick up extra hourswithout committing to a fixed full-time schedule. Prior clinical-trial experience is a plus butnot required—we will train motivated providers on study-specific procedures and GCP requirements.

Key Responsibilities

• Conduct study-relatedphysical examsand targeted assessments under the direction of the Principal Investigator (PI)
• Administer and/or overseeinvestigational product dosing, vaccinations, and sample collection
• Evaluate and documentadverse events (AEs), concomitant medications, and protocol deviationsin compliance with FDA/GCP guidelines
• Review lab results, ECGs, and other safety data; escalate abnormalities to the PI
• Ensure accurate, timely completion ofsource documentation and electronic case report forms (eCRFs)
• Collaborate with CRCs, regulatory staff, and other Sub-Is to keep each study audit-ready

Required Qualifications

• Active Nurse Practitioner or Physician Assistant license in Connecticut
• Minimum 2 years of direct patient care experience (primary care, urgent care, hospital, or similar)
• Current BLS certification; ACLS or PALS a plus
• Comfort with injections and routine outpatient procedures
• Strong EMR / computer skills and meticulous charting habits
• Availability to work weekday daytime hours with a few days prior notice (exact days/times vary by study visit schedule)

Preferred (Not Mandatory)

• Prior involvement in clinical research (e.g., sub-I, CRC, or study clinician)
• Familiarity with GCP, ICH guidelines, or IATA regulations
• Hourly rate: $75 – $90 (depending on experience) + paid orientation/training time
• Malpractice coverage provided for study-related services
• Rapid onboarding with paid GCP and protocol-specific training
• Opportunity to convert to a larger clinical research role as study volume grows

We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.