Principal Investigator Clinical Trials PT (Psych)
Company: Evolution Research Group
Location: Staten Island
Posted on: April 1, 2026
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Job Description:
About Company: Evolution Research Group (ERG) is dedicated to
delivering high-quality Phase I–IV clinical trial execution to help
sponsors bring lifesaving and life-enhancing therapies to market
quickly and safely. Founded in 2014, ERG has grown into a leading
neuroscience clinical development company, with affiliate sites
across the U.S. and deep expertise in clinical pharmacology,
psychiatry, neurology, acute pain, and metabolic disorders. ERG has
completed over 5,000 trials and continues to expand into high-need
therapeutic areas in the U.S. and globally. Why join us? We offer a
supportive culture, meaningful work, and the opportunity to
contribute to cutting-edge research alongside industry leaders.
Plus, we offer competitive benefits include medical and dental
coverage, a matching 401(k), and paid time off to recharge. Job
Description: RBA is looking for a psychiatrist who will serve as a
Principal Investigator to join their team on a PT basis, M-F . The
PI ensures adherence to protocol requirements, protecting the
rights and welfare of study subjects, assuring the integrity of
data generated at the site. In executing these position
responsibilities, the Investigator is guided by and promotes the
adherence to FDA regulations, Good Clinical Practice (GCP), and
company standard operating procedures and policies. The ideal
candidate will be a Family Medicine or Internal Medicine Physician.
Responsibilities: Employee Mentoring Responsibilities Work with the
Site Director and Medical Director to provide oversight of
Sub-Investigator. Review work to ensure adherence to SOPs, ICH GCP
guidelines, and protocol requirements. Protocol Planning and
Oversight Work with Site Director, Study Coordinator, and
Recruitment Manager to develop effective programs for study
enrollment. Work with Site Director to ensure that all staff are
adequately trained and adhere to Standard Operating Procedure and
working guidelines while performing study procedures on assigned
studies. Work with the Site Director to ensure the site has an
adequate number of qualified staff, adequate facilities, and that
the PI has adequate time to conduct the study. Maintain a current,
up to date curriculum vitae. Maintain current licensure to
practice. Oversee all trial-related medical decisions or ensure
that a qualified sub-investigator is available to do so. Assess
subject compliance with the test article and follow-up visits.
Assess subject's response to therapy. Evaluate for adverse
experiences per protocol guidelines. Assist with rating scales.
Provide new information about the study or test article(s).
Document deviations from the approved protocol. Document and
explain premature unblinding of the investigational product(s).
Thoroughly familiar with the use of the investigational product(s).
Communicate effectively with subjects, research team, IRB, and
sponsor. Skills and Qualifications: Education and experience M.D,
D.O., or PhD required. Requirements Able to communicate with
providers, co-workers, sponsors, and others in a collaborative and
courteous manner. Knowledgeable in medical terminology to
communicate with physician office and laboratory staff. Skilled in
working with potential sponsors to place research with the site.
Work effectively with a staff of clinical professionals and creates
a productive, satisfying work environment. Demonstrate the ability
to initiate activity as required and making appropriate decisions
within the constraints of study protocols and, regulatory
requirements. Able to initiate or modify behavior to achieve
desired outcomes despite environmental factors, priorities, or
problems that might not be well defined or that are subject to
change. Experienced negotiation skills Formal presentation skills
Excellent persuasive/selling skills. Understand regulatory
requirements, as well as Good Clinical Practices (GCP) and
International Conference of Harmonization (ICH) guidelines.
Excellent communication skills (interpersonal, written, verbal)
Basic computer skills to include Word, Excel, as well as
proprietary applications unique to the clinical research industry
(such as Study Manager)
Keywords: Evolution Research Group, Philadelphia , Principal Investigator Clinical Trials PT (Psych), Science, Research & Development , Staten Island, Pennsylvania
