Sub Investigator - Clinical Trials - Staten Island, NY

Hawthorne Health•Staten Island, NY

3d•Hybrid

About The Position

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. The role involves assisting the Principal Investigator (PI) in managing clinical trials, ensuring adherence to protocols and regulations, and providing medical oversight for study participants. Responsibilities include performing patient assessments, reviewing diagnostic tests, assisting with medical decisions, ensuring accurate data collection, and communicating with study teams and regulatory bodies. The position also requires assisting with investigational product management and participating in site visits and audits. Continuous medical education is expected to stay current with advancements in clinical research.

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.
Commitment to ethical conduct and patient safety.

Nice To Haves

Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus.

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.