Psychiatrist

Adams Clinical•New York, NY

8h•$300,000 - $500,000•Onsite

About The Position

Adams Clinical is a leading clinical trial site network dedicated to accelerating the development of life-changing medicines. Our mission is to deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare, with a vision to set the gold standard for clinical trial excellence. The company fosters a culture of respect, transparency, and continuous improvement, offering opportunities for professional growth and learning within a team committed to improving lives through innovation and integrity. Adams Clinical is seeking a Psychiatrist to serve as Principal Investigator (PI) at its New York research sites. The PI acts as the senior medical and scientific leader of the site, bearing responsibility for participant safety, protocol fidelity, and ensuring studies are conducted with accuracy, integrity, and adherence to regulatory standards. This role involves performing or overseeing key study assessments, reviewing safety data, confirming eligibility, managing adverse events (AEs) and serious adverse events (SAEs), and collaborating closely with clinical operations and other clinician staff. The position requires an engaged and collaborative physician who is present onsite, responsive to operational needs, and dedicated to upholding Adams Clinical’s standards of scientific rigor and participant-centered care.

Requirements

Serve as Principal Investigator (PI)
Engaged and collaborative physician who is present onsite, responsive to operational needs, and committed to maintaining Adams Clinical’s standards of scientific rigor and participant-centered care
Completing required certifications (for study rating scales)

Nice To Haves

Both psychiatric and Alzheimer’s disease experience
Prior research experience

Responsibilities

Conduct psychiatric/neurological evaluations, physical exams, and safety assessments
Confirm eligibility and support randomization decisions
Review labs, ECGs, and safety data; provide appropriate medical management
Perform study rating scales after completing required certifications
Ensure high-quality documentation aligned with ICH-GCP and FDA expectations
Serve as primary clinical contact for sponsors and CROs
Collaborate with operations to support trial recruitment, screening, and enrollment