Podsumowanie roli od JobGrid
Sub Investigator - Clinical Trials is an on-site Senior Healthcare & Science role with Hawthorne Health in Staten Island, United States. JobGrid presents the role as normalized structured facts, keeps the source boundary intact, and sends candidates to the original public application page with non-personal referral parameters. Source freshness is shown from the posted and last-checked timestamps; no salary is provided in the payload.
- On-site Senior Healthcare & Science role at Hawthorne Health in Staten Island, United States.
- Posted on 2026-06-02 and last checked on 2026-06-03.
- Salary is not provided in the source payload.
- Applications route to Hawthorne Health's original public application page with non-personal referral parameters.
Responsibilities
- 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 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.
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.