Psychiatrist / Sub-Investigator – Clinical Research (Part-Time, NYC)
@ Fieve Clinical ResearchPsychiatrist / Sub-Investigator – Clinical Research (Part-Time, NYC)
About the job
Fieve Clinical Research with over 40 years' experience conducts psychiatry and neurology trials, collaborating with top pharma companies, offering flexibility and training for clinicians.
Requirements
- MD or DO from an accredited school
- Active NY medical license
- Board certified/eligible in Psychiatry or Neurology
- Able to work 1+ days/week in Midtown Manhattan
- Basic understanding of clinical trial regulation
Qualifications
- 1-3+ years industry trial experience
- Experience with MDD or bipolar disorder
- Existing DEA registration or willing to obtain
- Spanish language skills
- Familiar with EDC systems
Full 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 - | fieveclinicalresearch.com
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