Since 1875, South Brooklyn Health has established its reputation for clinical excellence and culturally competent care. It has designations as a Certified Percutaneous Coronary Intervention (PCI) Center, an Advanced Primary Stroke Center, an accredited Baby-Friendly Hospital, a U.S. News & World Report high performing hospital. The hospital's staff is as diverse as the patients they serve. Interpreter services can be provided at any time of the day or night in over 130 languages.
At NYC Health + Hospitals, our mission is to deliver high quality care health services, without exception. Every employee takes a person-centered approach that exemplifies the ICARE values (Integrity, Compassion, Accountability, Respect, and Excellence) through empathic communication and partnerships between all persons.
Job Description
Purpose:
Reporting directly to the Director of Research, this person will work closely with Principal Investigators (PI) and study co-investigators (co-I) in the coordination of industry-sponsored and investigator-initiated clinical trials and projects. This person will be responsible for coordinating daily clinical trial activities, and will play a critical role in the conduct and approval of clinical trials within all Departments at SBH. The position requires a high level of organizational skills, analytical skills, and the ability to work independently.
Specific Duties And Responsibilities
The Associate Director (Hosp) Lv III is charged with and responsible for:
Specific Duties As Related To Clinical Trials
Schedules study subjects’ appointments and serves as the patient liaison to the PI and co-Is.
Reviews and comprehends clinical trial protocols including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
Possess thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
Coordinates and attends sponsor prequalification visits, monitor visits, study termination visits.
Complete and submit case report forms (CRFs) to study sponsors.
Responds to data clarification requests from sponsors in a timely manner.
Attend industry-sponsored investigator meetings requiring travel (or via Webex) and report pertinent information back to research team members.
Coordinate with PIs to ensure that clinical research and related activities are performed in accordance with Federal regulations, Institutional Review Board (IRB) and internal hospital policies and procedures.
Maintain subject screening logs and protocol deviation logs.
Maintain an Access database of all subjects enrolled on clinical trials.
Coordinate and facilitate monitoring and auditing visits.
Collaborate with PI to respond to audit findings and implement approved recommendations.
Complete documentation on each study visit that is used to track all study related activities.
Ensures that all materials for each clinical trial protocol are available for subject enrollment.
Performs specimen processing and shipment of biological specimen duties as needed.
Assists with study materials including but not limited to, the informed consent document, CRFs, enrollment logs, and drug/device accountability logs.
Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required.
Arranges secure storage of study documents that will be maintained according to institutional policy or for the contracted length of time, whichever is longer.
Maintain BRANY IRB approvals.
Obtain internal study approval through the NYC/H+H “System to Track and Approve Research” (“STAR”) program.
Assist physicians, nurses, and other research investigators in the research approval process.
Other job related duties as required.
Specific Duties Related To Resident-led Research
Provide guidance during protocol writing, IRB submission process and STAR submission process.
Assist the Director of Research with all tasks related to monthly research meetings and annual research fair.
Provide timely communication with all parties conducting research.
Keep a database of all resident/fellow led projects by departments and provide an oversight of their activities; monthly report to the Director of research in regards to the status of all IRB-approved projects.
Minimum Qualifications
Master’s degree from an accredited college or university in Hospital Administration, Health Care Administration, Public Health or a related discipline; and
Four (4) years of administrative experience and background at responsible management and administrative levels; or
An equivalent combination of training, educational background and experience in related fields and educational disciplines may be substituted on a year-for-year basis.
Department Preferences
Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors.
Knowledge of medical terminology a plus.
Excellent organizational skills to manage work flow independently.
Ability to prioritize quickly and appropriately.
Ability to multi-task.
Meticulous attention to detail
Ability to handle highly confidential information.
Experience utilizing Electronic Medical Records.
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies.
Proficiency in Microsoft Visio, Access, Publisher, Word, Excel, and PowerPoint is a must.
Knowledge of fundamentals of hospital organization, administration and standards, regulations and laws applicable to hospital operations. Knowledge of principles of business and personnel administration, management.
How To Apply
If you wish to apply for this position, please apply online by clicking the \"Apply for Job\" button.
NYC Health and Hospitals offers a competitive benefits package that includes:
Comprehensive Health Benefits for employees hired to work 20+ hrs. per week
Retirement Savings and Pension Plans
Loan Forgiveness Programs for eligible employees
Paid Holidays and Vacation in accordance with employees' Collectively bargained contracts
College tuition discounts and professional development opportunities
Multiple employee discounts programs
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NYC Health + Hospitals is the nation’s largest public health care delivery system. We are an integrated network of hospitals, trauma centers, neighborhood health centers, nursing homes, and post-acute care centers. We are a home care agency and a health plan, MetroPlus. The health system provides essential services to more than 1.4 million New Yorkers every year in more than 70 patient care locations and in their homes. Our talented workforce of more than 40,000 represents the diversity of our city and the communities we serve. The excellence of our staff, and our continued mission to care for all without exception, make us unique and rightly positioned to provide equitable, high-quality, culturally responsive, and affordable health care in every New York City community.
Our promise to New Yorkers: Empower every New Yorker – without exception – to live the healthiest life possible by providing equitable, high quality, culturally responsive, and affordable health care in every community.
Since 1875, South Brooklyn Health has established its reputation for clinical excellence and culturally competent care. It has designations as a Certified Percutaneous Coronary Intervention (PCI) Center, an Advanced Primary Stroke Center, an accredited Baby-Friendly Hospital, a U.S. News & World Report high performing hospital. The hospital's staff is as diverse as the patients they serve. Interpreter services can be provided at any time of the day or night in over 130 languages.
At NYC Health + Hospitals, our mission is to deliver high quality care health services, without exception. Every employee takes a person-centered approach that exemplifies the ICARE values (Integrity, Compassion, Accountability, Respect, and Excellence) through empathic communication and partnerships between all persons.
Job Description
Purpose:
Reporting directly to the Director of Research, this person will work closely with Principal Investigators (PI) and study co-investigators (co-I) in the coordination of industry-sponsored and investigator-initiated clinical trials and projects. This person will be responsible for coordinating daily clinical trial activities, and will play a critical role in the conduct and approval of clinical trials within all Departments at SBH. The position requires a high level of organizational skills, analytical skills, and the ability to work independently.
Specific Duties And Responsibilities
The Associate Director (Hosp) Lv III is charged with and responsible for:
Specific Duties As Related To Clinical Trials
Schedules study subjects’ appointments and serves as the patient liaison to the PI and co-Is.
Reviews and comprehends clinical trial protocols including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
Possess thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
Coordinates and attends sponsor prequalification visits, monitor visits, study termination visits.
Complete and submit case report forms (CRFs) to study sponsors.
Responds to data clarification requests from sponsors in a timely manner.
Attend industry-sponsored investigator meetings requiring travel (or via Webex) and report pertinent information back to research team members.
Coordinate with PIs to ensure that clinical research and related activities are performed in accordance with Federal regulations, Institutional Review Board (IRB) and internal hospital policies and procedures.
Maintain subject screening logs and protocol deviation logs.
Maintain an Access database of all subjects enrolled on clinical trials.
Coordinate and facilitate monitoring and auditing visits.
Collaborate with PI to respond to audit findings and implement approved recommendations.
Complete documentation on each study visit that is used to track all study related activities.
Ensures that all materials for each clinical trial protocol are available for subject enrollment.
Performs specimen processing and shipment of biological specimen duties as needed.
Assists with study materials including but not limited to, the informed consent document, CRFs, enrollment logs, and drug/device accountability logs.
Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required.
Arranges secure storage of study documents that will be maintained according to institutional policy or for the contracted length of time, whichever is longer.
Maintain BRANY IRB approvals.
Obtain internal study approval through the NYC/H+H “System to Track and Approve Research” (“STAR”) program.
Assist physicians, nurses, and other research investigators in the research approval process.
Other job related duties as required.
Specific Duties Related To Resident-led Research
Provide guidance during protocol writing, IRB submission process and STAR submission process.
Assist the Director of Research with all tasks related to monthly research meetings and annual research fair.
Provide timely communication with all parties conducting research.
Keep a database of all resident/fellow led projects by departments and provide an oversight of their activities; monthly report to the Director of research in regards to the status of all IRB-approved projects.
Minimum Qualifications
Master’s degree from an accredited college or university in Hospital Administration, Health Care Administration, Public Health or a related discipline; and
Four (4) years of administrative experience and background at responsible management and administrative levels; or
An equivalent combination of training, educational background and experience in related fields and educational disciplines may be substituted on a year-for-year basis.
Department Preferences
Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors.
Knowledge of medical terminology a plus.
Excellent organizational skills to manage work flow independently.
Ability to prioritize quickly and appropriately.
Ability to multi-task.
Meticulous attention to detail
Ability to handle highly confidential information.
Experience utilizing Electronic Medical Records.
Knowledge of good clinical practice, FDA, OHRP, HIPAA policies.
Proficiency in Microsoft Visio, Access, Publisher, Word, Excel, and PowerPoint is a must.
Knowledge of fundamentals of hospital organization, administration and standards, regulations and laws applicable to hospital operations. Knowledge of principles of business and personnel administration, management.
How To Apply
If you wish to apply for this position, please apply online by clicking the "Apply for Job" button.
NYC Health and Hospitals offers a competitive benefits package that includes:
Comprehensive Health Benefits for employees hired to work 20+ hrs. per week
Retirement Savings and Pension Plans
Loan Forgiveness Programs for eligible employees
Paid Holidays and Vacation in accordance with employees' Collectively bargained contracts
College tuition discounts and professional development opportunities