StaffAttract
  • Login
  • Create Account
  • Products
    • Private Ad Placement
    • Reports Management
    • Publisher Monetization
    • Search Jobs
  • About Us
  • Contact Us
  • Unsubscribe

Login

Forgot Password?

Create Account

Job title, industry, keywords, etc.
City, State or Postcode

Principal Investigator in Clinical Research (Licensed ...

Brooklyn Clinical Research - Brooklyn, NY

Apply Now

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.Pay: $290,000.00 - $320,000.00 per yearBenefits:* 401(k)* 401(k) matching* Dental insurance* Health insurance* Paid time off* Vision insuranceWork Location: In person

Created: 2025-12-31

➤
Footer Logo
Privacy Policy | Terms & Conditions | Contact Us | About Us
Designed, Developed and Maintained by: NextGen TechEdge Solutions Pvt. Ltd.