About Job
About Clindove Research
We’re an independent, fast‑growing clinical research site in Brooklyn helping the local community through clinical research!
The Opportunity
You’ll start as a Sub‑Investigator supporting our lead Principal Investigator on upcoming study protocols. You’ll handle subject eligibility, safety oversight, and data integrity while learning the full PI skill‑set. Once you’ve logged sufficient study experience, we can transition to making you a Principal Investigator on a future study.
Core Responsibilities
- Conduct psychiatric evaluations, obtain informed consent, and determine study eligibility
- Perform/oversee study visits, AE/SAE assessments, and concomitant‑med reviews
- Collaborate with CRCs on source documentation & EDC entries
- Participate in Site Initiation Visits (SIVs), monitoring visits, and audits
- Uphold GCP & FDA investigator responsibilities to protect subjects and ensure data quality
- Mentor future staff and contribute to SOP development as we grow
What We’re Looking For
- MD/DO with completed psychiatry residency; board‑certified
- New York medical license (or ability to obtain within 60 days)
- Clinical research exposure a plus but not required
- Comfortable working 2-3 weekdays on‑site; open to expanding hours as pipeline grows
- Pro-active mindset—enjoys building systems, solving problems, and seizing new trials
- Excellent bedside manner and documentation discipline
Job Type: Part-time
Pay: $100,000.00 - $200,000.00 per year
Application Question(s):
- How many industry sponsored trials have you been an investigator for?
Ability to Commute:
- Brooklyn, NY 11221 (Required)
Ability to Relocate:
- Brooklyn, NY 11221: Relocate before starting work (Required)
Work Location: In person
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