What are the responsibilities and job description for the Sub-Investigator (MD or DO) in Clinical Research with Growth to Principal Investigator position at Brooklyn Clinical Research?
Sub-Investigator in Clinical Research (MD or DO) – 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 or DO who has completed residency in the United States to join our team as sub investigator (“Sub-I”) in clinical research at our Brooklyn office. The Sub-I will work with our Principal Investigator (“PI”) to conduct all clinical trials according to the study protocol, ICH, GCP, and local regulations. We expect that the Sub-I role should lead to a PI role within 6 to 9 months of employment.
As a Sub-Investigator, you will work closely with the PI to conduct clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This role is ideal for physicians looking to expand their expertise into clinical research while contributing to groundbreaking medical advancements.
This is a full-time, in-person role. The target start date for this role is April or May 2025, depending on the candidate’s availability.
Responsibilities include but are not limited to :
- Managing the informed-consent process.
- Evaluating and screening potential participants based on the inclusion and exclusion criteria in the study protocols.
- Conduct medical assessments, including physical examinations and evaluations, to determine participant eligibility and safety.
- Interpreting study protocols and strategizing with PI and management on participant recruitment.
- Following trial protocols in accordance with FDA regulations and ICH / GCP Guidelines.
- Provide medical expertise to address study-related questions and ensure participant safety.
- Collaborate with the study team to monitor and document participant progress and report Adverse Events (“AEs”) and Serious Adverse Events (“SAEs”).
- Maintaining all required licenses to practice.
- Completing all required documentation in accordance with the study protocol and adherence to FDA Form 1572.
- Collaborating with other members of the team, including clinical research coordinators and office management.
- Maintaining accurate and detailed source records to ensure data integrity.
- Staying up to date on the latest medical research and advances in the field.
- Attending investigator meetings as needed.
Requirements :
Comprehensive benefits package including health insurance, dental insurance, and vision insurance; paid time off, sick days, and paid holidays; and 401(k) with employer contributions.
Please submit a cover letter along with your resume.