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Principal Investigator (Clinical Research)
Principal Investigator (Clinical Research)Brooklyn Clinical Research • New York, NY, US
Principal Investigator (Clinical Research)

Principal Investigator (Clinical Research)

Brooklyn Clinical Research • New York, NY, US
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Job Description

Principal Investigator (Clinical Research)

Company : Brooklyn Clinical Research

Location : Brooklyn, NY (In-person)

Job Type : Full-time

Company Overview

Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented communities. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals.

Job Overview

We are seeking to hire a board-certified MD to join our team as a Principal Investigator (“PI”) at our Brooklyn office. The PI will oversee clinical trials primarily in Phase 2 and Phase 3, focusing on high-impact therapeutic areas including Obesity, GLP-1s, Pain Management, Vaccines, and Cardiometabolic health.

The ideal candidate has a background in Internal Medicine or Family Medicine, has completed their residency in the United States, and possesses previous research experience. You will conduct trials according to study protocols, ICH / GCP guidelines, and local regulations while ensuring patient safety and data integrity.

Responsibilities

  • Study Oversight : Administer trial protocols in accordance with FDA regulations, ICH / GCP Guidelines, and standard operating procedures.
  • Patient Safety : Oversee all participant visits, monitoring for Adverse Events (“AEs”) and Serious Adverse Events (“SAEs”), and ensuring patient well-being throughout the trial.
  • Recruitment & Screening : Interpret study protocols and strategize with management on participant recruitment; evaluate and screen potential participants based on specific inclusion and exclusion criteria.
  • Informed Consent : Directly oversee the informed-consent process to ensure participants are fully educated on the study.
  • Documentation : Complete all required documentation in accordance with study protocols and FDA Form 1572; maintain accurate and detailed records to ensure data integrity.
  • Collaboration : Collaborate with Clinical Research Coordinators (CRCs) and office management to ensure smooth site operations.
  • Professional Development : Stay up to date on the latest medical research and advances in the field; attend investigator meetings as needed.
  • Licensure : Maintain all required licenses to practice in the state of New York.

Requirements

  • Education & Licensure : Must hold an active MD license to practice in New York State.
  • Residency : Must have completed residency in the United States .
  • Specialty : Board certification in Internal Medicine or Family Medicine is strongly preferred.
  • Experience : Prior research experience as a Principal Investigator (PI) or Sub-Investigator (Sub-I) is required .
  • Skills : Strong communication skills and a history of providing compassionate patient care.
  • Attributes : Meticulous attention to detail regarding data entry, regulatory documentation, and safety reporting.

    • Compensation & Benefits

  • Base Salary : $290,000 - $320,000 per year, depending on experience and specialty.
  • Incentives : Potential for a performance-based bonus plan.

    • Benefits :

  • Comprehensive health, dental, and vision insurance.
  • 401(k) with employer matching.
  • Paid time off and paid holidays.
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