Brooklyn Clinical Research
Principal Investigator (Clinical Research)
Brooklyn Clinical Research, New York, New York, us, 10261
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.
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.
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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.
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.
#J-18808-Ljbffr