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Psychiatrist / Sub-Investigator Clinical Research (Part-Time, NYC)
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What they do
A Clinical Investigator works on a clinical trial, and is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.
$159,330 / year median in New York
+12% projected growth
Job Description
Fieve Clinical Research is seeking a second board-certified physician to serve as Sub-Investigator (Sub-I) or Co-Principal Investigator on active and upcoming Phase II-IV clinical trials in psychiatry and neurology. This is an ideal fit for a psychiatrist, neurologist, or internist
- including residents, academic faculty, or clinicians transitioning from industry
- who wants to stay connected to drug development without a full-time research commitment. About Us Founded on the legacy of Ronald R. Fieve, MD
- the Columbia University psychiatrist who established lithium therapy for bipolar disorder in the U.S.
- Fieve Clinical Research has been part of Manhattan's clinical research landscape for more than 40 years.
Our investigators have conducted 125+ trials across psychiatry, neurology, pain management, and internal medicine, working with major pharmaceutical sponsors and leading CROs including IQVIA and ICON. What You'll Do Serve as Sub-I or Co-PI on industry-sponsored outpatient trials (MDD, GAD, TRD, PTSD, migraine, fibromyalgia, and more) Conduct protocol-specified medical/psychiatric evaluations and administer validated rating scales (MADRS, HAM-D, CGI, MIDAS, HIT-6) Review subject eligibility, informed consent, and safety decisions Identify and report adverse events per
FDA/ICH-GCP
requirements Maintain GCP-compliant source documentation Participate in site initiation visits, monitoring visits, and audits as assigned Partner with the PI and Site Director on feasibility and enrollment strategy Provide mentorship to study coordinators as your involvement grows Why This Role Minimum 1 day/week, Saturdays available
- built around your existing clinical or academic schedule No prior research experience required
- we provide GCP training and mentorship Authorship and CV-building potential on active industry trials Direct path into psychopharmacology research at a site with a 40-year track record Qualifications
- Required MD or DO from an accredited medical school Active, unrestricted New York State medical license Board certified or board eligible (NY) in Psychiatry, Neurology, or a closely related specialty; internists also considered Ability to commit to a minimum of 1 on-site day/week in Midtown Manhattan Baseline familiarity with clinical trial regulatory requirements (FDA, IRB, informed consent) ICH-GCP certification preferred but not required•we support training/renewal Qualifications•Preferred 1-3+ years as a sub-investigator or investigator on industry-sponsored trials (not required•training provided) Experience with MDD, bipolar disorder, schizophrenia, migraine, or epilepsy Existing DEA registration, or willingness to obtain Spanish language proficiency Familiarity with EDC systems (Medidata Rave, Oracle InForm, REDCap) Fieve Clinical Research is an Equal Opportunity Employer.
All qualified applicants will receive consideration regardless of race, color, religion, sex, national origin, disability, or veteran status.
HOW TO APPLY
Please send your CV/biosketch, a brief cover note on your research background and therapeutic interests, and confirmation of your NY license/board status to: Liana Slater, Operations
- liana.
slater@fieveclinical.com (347) 281-3998 | fieveclinicalresearch.com Contact Information Please click APPLY!