Principal Investigator (Clinical Research) (Brooklyn)Brooklyn Clinical Research • Brooklyn, NY, US
Principal Investigator (Clinical Research) (Brooklyn)
Brooklyn Clinical Research • Brooklyn, NY, US
[job_card.1_day_ago]
[job_preview.job_type]
- [job_card.full_time]
- [job_card.part_time]
[job_card.job_description]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. Base Salary : $290,000 - $320,000 per year, depending on experience and specialty. Incentives : Potential for a performance-based bonus plan. Comprehensive health, dental, and vision insurance. 401(k) with employer matching. Paid time off and paid holidays.
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
Compensation & Benefits
Benefits :
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Principal Investigator • Brooklyn, NY, US
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