Sub Investigator - Clinical Trials - Staten Island, NY

About the role

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster. Hawthorne Health is seeking a Nurse Practitioner (NP) or Certified Physicians Assistant (PA-C) with experience supporting sponsor initiated trials as a Principal or Sub-Investigator to oversee clinical trials at our site in Staten Island, NY. Site Address: 6400 Amboy Rd. Staten Island, NY 10309 Why Hawthorne Health? At Hawthorne Health, you'll be joining a fast-growing clinical research organization that is redefining how patients access clinical trials. As a Sub-Investigator, you'll work across diverse therapeutic areas, collaborate with experienced research professionals, and play a key role in expanding research opportunities within local communities. If you're looking for a position where you can make an impact, continue to grow professionally, and be part of an organization on the leading edge of community-based research, we'd love to hear from you.

Requirements

• Must have an active Nurse Practitioner or Physician Assistant license in New York.
• Experience working on at least 3 sponsor initiated clinical trials as an 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.

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